Tag: recall

FDA upgrades recall of frozen blueberries sold at Publix to highest health risk level

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Pile of fresh blueberries on a wooden table beside a spoon

The Food and Drug Administration upgraded a recall of frozen blueberries and mixed berries sold at Publix grocery stores across the U.S. to the highest health risk level on Tuesday, according to an enforcement report.  Publix on July 29 announced a recall of four varieties of frozen GreenWise organic blueberries and mixed berries sold at stores across eight states over potential E. coli contamination. The FDA is now categorizing it as a “Class 1” recall, which the agency assigns to product recalls “in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.”

Twelve people infected with the outbreak strain of E. coli have been reported in two states, according to the Centers for Disease Control and Prevention. No deaths linked to the outbreak have been reported.  The following products, shipped to Publix stores in Alabama, Florida, Georgia, Kentucky, North Carolina, South Carolina, Tennessee and Virginia, are under recall. They should be discarded or returned to Publix for a full refund. Their expiration dates are before Feb. 9, 2028.

  • GreenWise Organic Whole Blueberries, 10-ounce, UPC 41415-06453
  • GreenWise Organic Whole Blueberries, 48-ounce, UPC 41415-12053
  • GreenWise Organic Whole Mixed Berries, 10-ounce, UPC 41415-06753
  • GreenWise Organic Whole Mixed Berries, 48-ounce, UPC 41415-12153

E. coli, a large group of bacteria, can cause illness characterized by severe stomach cramps, diarrhea and vomiting, according to the FDA. In severe cases, the bacteria can cause hemolytic uremic syndrome, which can lead to kidney failure and be life-threatening.  Last week, the FDA also upgraded an egg recall to the highest health risk level over potential salmonella contamination.

Source: FDA upgrades recall of frozen blueberries sold at Publix to highest health risk level – CBS News

For in it the righteousness of God is revealed from faith to faith; as it is written, “The just shall live by faith.”
Romans 1:17

Powerful earthquake shakes Panama

A major earthquake with a preliminary magnitude of 7.7 has struck Panama, according to the US Geological Survey. Local media are reporting structural damage in some parts of the…

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Plague in Russia?

Russian authorities have sought to allay global worries over the death of a young woman who worked at a Siberian anti-plague laboratory. But moves to isolate her contacts and…

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Nearly 30,000 pounds of Argentine beef sold in Texas, Florida recalled by Miami-area company

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Vacuum-sealed Argentine beef ribeye cuts with SENASA inspection labels

Shoppers in Texas and Florida are being asked to check their freezers for beef imported from Argentina that is now being recalled by federal officials. The Food and Drug Administration’s Food Safety and Inspection Service (FSIS) announced Friday that Corte Argentino – a company based in Aventura, Florida – recalled nearly 30,000 pounds of raw beef products produced in May that have use or freeze-by dates between Sept. 15, 2026, and Sept. 20, 2026. The FSIS said the products were imported without the benefit of import reinspection into the United States. The service said the issue was discovered during routine inspection activities. Five products, all of which are boneless beef products in cardboard boxes of various weights and carry the “FrigorIfico Gorina SAIC” brand, are impacted:

  • “Top Sirloin Butt” (“Cuadril Sin Tapa”)
  • “Eye Round” (“Peceto”)
  • “Topside Cap Off” (“Nalga AD S/Tapa”)
  • “Flat” (“Carnaza Cuadrada”)
  • “Knuckle” (“Bola de Lomo”)

CBS News

Texas The FSIS said the products subject to the recall bear Argentine establishment number “EST. N° OF. 2025” and shipping mark “26644-AA”. While it’s not known which stores may have sold the beef, the service said the products were distributed to distributors and retailers in both states. While no illnesses or injuries have been reported as a result of eating the beef, the FSIS urges anyone with concerns to contact a healthcare provider. The service also said anyone who still has the beef should either throw it away or return it to the place of purchase. Anyone with questions about the recall can email Corte Argentino at info@corteargentinoinc.com.

Recall comes after U.S. ranchers’ opposition The recall of the Corte Argentino beef comes nearly a year after President Donald Trump announced a plan to import more meat from Argentina as part of a deal signed with his counterpart, Argentine President Javier Milei, as part of a plan to cut record beef prices. However, that plan was met with heated opposition from U.S. ranchers and skepticism from experts who said it likely wouldn’t lead to lower prices at grocery stores. The National Cattlemen’s Beef Association, along with the Ranchers-Cattlemen Action Legal Fund United Stockgrowers of America and other farming groups — who are normally some of the president’s biggest supporters — all criticized Trump’s plan because of what it could do to American ranchers and feedlot operators. And agricultural economists say Argentine beef accounts for such a small slice of beef imports — only about 2% — that even doubling that wouldn’t change prices much.  

Several factors have sent beef prices soaring, starting with continued strong demand combined with the smallest U.S. herd size since 1961. In part, that small herd is due to years of drought and low cattle prices. Further, Kansas State University agricultural economist Glynn Tonsor said Argentina can’t produce enough beef to offset those other losses of imports. “We’re always going to have uncertainty in the world. But the more uncertain something is, the less likely most are to put money on the line,” Tonsor said.

Source: Nearly 30,000 pounds of Argentine beef sold in Texas, Florida recalled by Miami-area company – CBS Texas

No one has seen God at any time. If we love one another, God abides in us, and His love has been perfected in us.
1 John 4:12

For God so Loved the World

“God loved you enough to send His Son, Jesus loved you enough to give His life, and through faith, you are offered a hope this world can never take…

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2 Timothy 3:12 

Indeed, all who desire to live a godly life in Christ Jesus will be persecuted Paul was reminding Timothy that following Christ does not guarantee an easy life. When we choose…

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John 15:18–20

“If the world hates you, know that it has hated me before it hated you. If you were of the world, the world would love you as its own; but…

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Galatians 1:6-10

“When truth becomes negotiable, faith becomes vulnerable so know the Gospel, stand on God’s Word, and seek His approval above the world’s applause.” “I am astonished that you are…

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1.3 million Ram trucks recalled over improperly installed seat belt anchors

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trunk parked on paved road covered with pebbles at sunset

Chrysler is recalling more than 1.27 million Ram 1500 pickup trucks because the second-row seat belt buckle anchors may have been improperly installed, according to the National Highway Traffic Safety Administration. The recall affects Ram 1500 trucks from the 2019 through 2026 model years. NHTSA said the anchors fail to meet federal safety standards. An improperly installed anchor may not properly restrain rear-seat passengers, increasing the risk of injury in a crash, according to the agency. Dealers will inspect the seat belt buckle anchors and reattach them to the vehicle’s body structure as needed, free of charge.

Chrysler said it plans to mail owner notification letters starting Aug. 18. Vehicle identification numbers included in the recall will be searchable at NHTSA.gov starting Aug. 6 under campaign number 26V495. Owners with questions can contact Chrysler customer service at 1-800-853-1403 and reference recall number 67D. They can also reach NHTSA’s Vehicle Safety Hotline at 1-888-327-4236.

Source: 1.3 million Ram trucks recalled over improperly installed seat belt anchors | whas11.com

Oh, taste and see that the LORD is good; Blessed is the man who trusts in Him!
Psalm 34:8

Isaiah 45:2

“I will go before you and level the exalted places, I will break in pieces the doors of bronze and cut through the bars of iron, This verse reminds us that…

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Proverbs 21:23

Whoever keeps his mouth and his tongue keeps himself out of trouble. This verse emphasizes that people who carefully watch what they say will protect themselves from serious trouble. “Guarding your…

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Slow to Speak: The Secret to Wise Reactions

Talk less, listen more, because wisdom speaks after it understands, not before. If you want stronger relationships and real influence, master this: control your tongue, calm your anger, and lead with…

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Psalm 5:8

Lead me, O Lord, in your righteousness because of my enemies; make your way straight before me. In the verse David is praying in the morning while people who hate him…

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Antihistamine recall across the U.S. triggered by heartburn drug contamination risk, FDA says

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open green pill bottle with white tablets on blue surface

A generic version of the brand-name allergy medication Zyrtec is under recall across the U.S. due to potential cross-contamination with a heartburn drug, according to the Food and Drug Administration.  Drugmaker Unique Pharmaceutical Laboratories is voluntarily recalling antihistamine drugs, commonly used to treat seasonal allergies, over potential cross-contamination with ranitidine, a heartburn drug. Unique Pharmaceutical Laboratories announced the recall on July 18.  A pharmacy technician observed what they described as a red dot on some of the antihistamine drugs — cetirizine hydrochloride tablets USP 5 mg — when counting and bottling the medications, according to the FDA’s recall notice.

Other tablets were discolored, alerting the technician to a possible issue.  The FDA indicated that consumers who are hypersensitive to ingredients contained in ranitidine could experience adverse side effects upon exposure, including hypotension, shortness of breath, difficulty swallowing, loss of consciousness and other life-threatening reactions.  There have been no reports of adverse events related to the recall, according to the FDA.  What products are affected?  The tablets, distributed by Rising Pharma Holdings Inc. to retailers across the U.S., are packaged in 100-tablet bottles. Products with the following lot numbers, set to expire in October 2028, are under recall:

  • GY825029
  • GY825030
  • GY825031
  • GY825032

Rising Pharmaceutical Holdings has notified its customers about the recall and is arranging for the return of all drugs that are under recall.  Consumers with questions can contact Rising Pharma Holdings directly at 1-844-874-7464, or by email at  pv@risingpharma.com  or qa@risingpharma.com. Patients are encouraged to reach out to their healthcare provider if they experience problems related to the potentially contaminated drugs. 

Source: Antihistamine recall across the U.S. triggered by heartburn drug contamination risk, FDA says – CBS News

But let him ask in faith, with no doubting, for he who doubts is like a wave of the sea driven and tossed by the wind.
James 1:6

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Ford recalls more than 250,000 Focus models due to engine stall risk

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News anchor reporting on Ford Focus recall alert with details on affected vehicles and issues

Ford is recalling more than 250,000 vehicles that were incorrectly repaired under a previous recall meant to fix a problem that caused the engine to stall while driving, according to the National Highway Traffic and Safety Administration. The recall includes 255,404 Ford Focus automobiles, model years 2012-2018. Ford said the canister purge valve may stick open, causing the engine to stall unexpectedly while driving, increasing the risk of a crash and injury. “Affected vehicles may illuminate a Malfunction Indicator Light (MIL) or customers may observe inaccurate fuel gauge indication, inaccurate distance to empty indication and/or have drivability concerns,” the federal agency said To fix the problem, dealers will provide a powertrain software update free of charge.

Owner notification letters are expected to be mailed between July 6 and July 10. Owners may contact Ford customer service at 1-866-436-7332 or a local Ford or Lincoln dealer to see if their vehicle is impacted. Ford’s number for this recall is 26S40. The federal agency’s number for this recall is 26V369. The original NHTSA recall number for this issue is 18V735. Vehicle identification numbers involved in this recall will become searchable on NHTSA.gov on July 6.

Source: Ford recalls more than 250,000 Focus models due to engine stall risk – CBS Detroit

He who is slow to anger is better than the mighty, And he who rules his spirit than he who takes a city.
Proverbs 16:32

A study of the Mesha Stele

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Target voluntarily recalling 2 types of baby wipes over contamination concerns

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News anchor at desk with recall alert for Up & Up baby wipes on screen

Target is voluntarily recalling two types of baby wipes due to concerns that the products may be contaminated with bacteria that may cause “serious and life-threatening infections,” the U.S. Food and Drug Administration said on Friday. The Minnesota-based company is recalling Up and Up Fragrance Free Baby Wipes and Up and Up Fresh Cucumber Scented Baby Wipes. The products are predominantly used on newborns, infants and young children who are vulnerable to infection due to their immature immune systems, the federal agency said.

The manufacturer of the wipes, Sapro Temizlik Urunleri, and the company received “a number of consumer complaints” alleging product discoloration and symptoms including skin and eye irritation, and infections “potentially associated with the use of the product,” according to officials. The agency then tested and identified the presence of Burkholderia cepacia complex and Burkholderia gladioli in product samples. “In healthy individuals, use of the product on skin with minor lesions will more likely result in local infections, whereas in immunocompromised individuals, newborns, infants and young children, the infection is more likely to spread into the bloodstream, potentially leading to life-threatening sepsis or pneumonia,” the agency said in a written statement.

The baby wipes were sold at Target stores nationwide and online at Target.com, the agency said. According to officials, the company is recalling the Up and Up Fragrance Free Baby Wipes with a manufacturing date code from Nov. 7, 2025, to May 5, 2026, and expiration dates between May 10, 2028, and Nov. 5, 2028, are being recalled in the following pack sizes  and universal product codes:

  • 20 Count: UPC 085239265956
  • 72 Count: UPC 085239265949
  • 216 Count: UPC 085239265963
  • 800 Count: UPC 085239266137
  • 1200 Count: UPC 085239266090

According to the agency, Up and Up Fresh Cucumber Scented Baby Wipes with a manufacturing code of Dec. 29 or Dec. 30, 2025, and expiration dates of June 29 or June 30, 2028, are being recalled in the following pack sizes and universal product codes:

  • 72 Count: UPC 085239265970
  • 216 Count: UPC 085239265994
  • 800 Count: UPC 085239265987

U.S. Food and Drug Administration Anyone with the recalled products should stop using them and return them to any Target store for a full refund, the agency said. Consumers with questions can call Target Guest Relations at 1-800-440-0680 anytime between 7 a.m. and 10 p.m. CT.

Source: Target voluntarily recalling 2 types of baby wipes over contamination concerns – CBS Minnesota

For I delivered to you first of all that which I also received: that Christ died for our sins according to the Scriptures, and that He was buried, and that He rose again the third day according to the Scriptures.
1 Corinthians 15:3-4

Finding Truth and Life in Jesus

In a world filled with competing voices, confusing paths, and endless distractions, Jesus doesn’t simply show us the way He declares, ‘I am the way.’ When everything around you…

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Organic formula brand issues recall after 3 babies diagnosed with infant botulism

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Global News anchors presenting breaking news on baby formula recall in studio

An organic baby formula is being voluntarily recalled after three infants who were fed the product were hospitalized with infant botulism, according to a notice from the Food and Drug Administration.  The Centers for Disease Control and Prevention confirmed that all three babies had consumed Nara Organics Powdered Infant Formula, which is sold at Target stores throughout the United States. The sickened babies were in California, Washington and Pennsylvania, according to the FDA notice. All three babies were successfully treated, and no deaths have been reported, the FDA said.  The products were also sold at Target.com and Nara.com.

The formula was not sold outside the United States, according to the FDA notice.  No lots of Nara Organics Powdered Infant Formula have tested positive for Clostridium botulinum, the bacteria that causes infant botulism, according to the FDA, but all whole milk infant powdered formula products are being recalled voluntarily by the company.  The three product lots consumed by the sickened babies are 709125280E14F2, 709125288E14F2 and 708125174E14F2, according to the FDA. The lot numbers can be found on the bottom of the formula cans.  Food and Drug Administration “Nara is taking aggressive action to ensure the safety of the babies and families who use the product as we work closely with the FDA, Centers for Disease Control and Prevention (CDC), and state partners to support their investigation into the root causes of these cases,” the company said in the FDA notice. 

Customers should stop using the affected products immediately, according to the notice. Anyone who purchased formula from Nara.com between May and June 2026 will receive an automatic refund. Others who bought it from Nara.com can request a refund online. Consumers who purchased the product at Target should return the product there or visit Target’s website for a refund.  Infant botulism occurs when Clostridium botulinum spores enter and colonize the intestinal tract, causing botulinum neurotoxins to grow there, according to the CDC. An outbreak of infant botulism tied to the formula brand ByHeart led to over 50 illnesses in 19 states. 

Affected babies may show symptoms including constipation, poor feeding, drooping eyelid, sluggish pupils, low muscle tone, difficulty sucking and swallowing, weak or altered crying, difficulty breathing, and generalized weakness. Respiratory arrest is also possible. The disease can be fatal.

Source: Organic formula brand issues recall after 3 babies diagnosed with infant botulism – CBS News

You are the salt of the earth. But if the salt loses its saltiness, how can it be made salty again? It is no longer good for anything, except to be thrown out and trampled underfoot.
Matthew 5:13

Hope in the dark

Pip: A mountain village, a wandering stranger, a mother weaving a basket by the river — Drink of Jesus has been building a world where ancient scripture lands like it’s happening…

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Blackstone recalls seasoning over salmonella contamination

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News anchor delivering breaking news about Blackstone recalling three seasoning products due to potential salmonella contamination

This recall includes three lots of the seasoning products sold nationwide at Walmart and on the Blackstone website.

Source: Blackstone recalls seasoning over salmonella contamination – CBS Chicago

Can one walk on hot coals, And his feet not be seared?
Proverbs 6:28

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Ice cream sold in 17 states recalled for potential metal fragments

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News broadcast announcing recall of Straus Family Creamery ice cream for potential metal contamination

Straus Family Creamery is voluntarily recalling a variety of organic ice cream flavors and sizes sold in 17 states because of concerns there may be metal fragments in the frozen treats, the Food and Drug Administration said Friday.  No injuries have been reported because of the issue, the FDA said.  The recall affects some products sold in Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Maryland, New Jersey, Oregon, Pennsylvania, South Carolina, Texas, Washington and Wisconsin. The affected items were on shelves beginning on May 4, the FDA said.  Pints of Straus Family Creamery’s dutch chocolate ice cream. Michael Macor/The San Francisco Chronicle via Getty Images The affected products can be determined by their best-by dates, the FDA said. Best-by dates are printed on the bottom of the container.

The recalled products include:  Vanilla bean pints with best-by dates of Dec. 23 and 28, 2026, with the manufacturing code 7-84830-10030-6.  Strawberry pints with a Dec. 25, 2026, best-by date and the manufacturing code 7-84830-10095-5.  Strawberry quarts with a Dec. 24, 2026, best-by date and the manufacturing code 7-84830-10097-9.  Cookie dough pints with a Dec. 26, 2026, best-by date and the manufacturing code 7-84830-10104-4.  Dutch chocolate quarts with a Dec. 27, 2026, best-by date and the manufacturing code 7-84830-10012-2.  Mint chip quarts with a Dec. 30, 2026, best-by date and the manufacturing code 7-84830-10050-4.

Straus Family Creamery is working with retailers to remove the affected products from shelves, the FDA said. Anyone who has purchased an affected container should dispose of the product.  Straus said it would not offer refunds, but would issue vouchers to interested customers so they can buy another carton. Voucher information is available on the company’s website. 

Source: Ice cream sold in 17 states recalled for potential metal fragments – CBS News

Blessed is the man Who walks not in the counsel of the ungodly, Nor stands in the path of sinners, Nor sits in the seat of the scornful.
Psalm 1:1

The Distraction of Fear

Fear has a way of making tomorrow feel more real than today. But you were never meant to live inside a future that hasn’t happened yet, you were called…

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Too Busy to Hear God

You can be so busy doing things for God that you never stop long enough to hear from God. Sometimes the biggest distraction in your life isn’t rebellion, it’s…

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Who Has Your Attention?

Your attention is one of the most valuable things you own, and everyone wants a piece of it. The question isn’t whether something is getting your attention—the question is…

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Costco electric kettle recalled after fire hazard leaves person burned

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Recall sign

More than 113,000 electric kettles sold at Costco and HomeGoods have been recalled after reports that the handles can detach and spill hot water, including one reported second-degree burn, according to the Consumer Product Safety Commission (CPSC). The recall, announced May 14, involves ZWILLING J. A. Henckels Aktiengesellschaft Enfinigy Kettle and Enfinigy Kettle Pro electric stainless-steel kettles after reports of the handles loosening and separating, posing a risk of serious injury due to a burn hazard. About 113,440 kettles were recalled in the United States, according to the CPSC report. An additional 43,963 were sold in Canada and 48 were sold in Mexico. The firm received 163 reports of kettle handles loosening or separating, including five incidents involving handle separation and one reported second-degree burn.

The affected kettles can be identified by model numbers 53101-200 and 53101-201 for the 1.5L ENFINIGY Electric Kettle, and 53101-500, 53101-501, 53101-502, 53101-503 and 53101-504 for the 1.5L ENFINIGY Electric Kettle Pro.

Source: Costco electric kettle recalled after fire hazard leaves person burned

Whoever has no rule over his own spirit Is like a city broken down, without walls.
Proverbs 25:28

Finding Strength in God

You don’t have to carry this alone, He is your safe place and your help in every moment of need.  Bible Verse:God is our Refuge and Strength…

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Good & Gather snack, other nut mixes recalled due to salmonella risk

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Recall notice for Good & Gather assorted snack mixes due to undeclared semolina allergen

An Illinois food manufacturer is recalling several snack products due to concerns that they may be contaminated with salmonella, according to a recall notice with the Food and Drug Administration. The recall affects nut mixes and a corn mix manufactured by John B. Sanfilippo and Son and sold under the brand names Southern Style Nuts, Fisher, Squirrel Brand and Good & Gather.  The Good & Gather product, a Mexican street corn-inspired trail mix, was sold at Target, while the others were sold at various retail stores, online and by QVC, according to the FDA notice.

Source: Good & Gather snack, other nut mixes recalled due to salmonella risk – CBS Sacramento

Surely He has borne our griefs And carried our sorrows; Yet we esteemed Him stricken, Smitten by God, and afflicted.
Isaiah 53:4

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RECALL: Infant formula batches from a2 Milk Company recalled over possible cereulide toxin, FDA says

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Recall notice for certain Similac, Alimentum, and Elecare baby formulas on an empty store shelf

The a2 Milk Company has voluntarily recalled three specific batches of infant formula after detecting a possible toxin, according to the U.S. Food and Drug Administration. The baby formula in question was sold via Amazon and at Meijer, the FDA said, in addition to the company’s website. The reason for the recall is “presence of cereulide toxin produced by some strains of the bacterium Bacillus cereus.” 

Source: Infant formula batches from a2 Milk Company recalled over possible cereulide toxin, FDA says – CBS Detroit

Treasures of wickedness profit nothing, But righteousness delivers from death.
Proverbs 10:2

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Ford recalls 144,000 F-150s in Canada due to gearshift issue

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powerful black pickup truck on a sunny day

Ford is issuing a safety recall for some 144,oo0 F-150s in Canada, the company said Friday, due to an issue with the vehicles’ gearshift that can impact the drivers’ control of the vehicle. The safety issue impacts some vehicles with six-speed automatic transmissions made between 2015 and 2017. In the U.S., almost 1.4 million vehicles are affected, including some 2014 model years as well. In some of the trucks, deteriorated electrical connections in the internal transmission lead frame can cause a signal issue from a transmission sensor, according to the company. “This may lead to an unexpected downshift into a lower gear while the vehicle is in motion,” a Ford spokesperson told CBC News in an emailed statement.

The U.S. National Highway Traffic Safety Administration’s safety recall report said the issue may cause an abrupt reduction in wheel speed for a short period of time, which in some situations could cause the rear tires to slide until the vehicle speed slows. The automaker is aware of two injuries and one accident possibly related to the issue, according to The Associated Press. Ford says dealers can update the vehicles’ Powertrain Control Module (PCM) software, which should fix the issue. Alternatively, if an affected vehicle previously displayed “specific diagnostic trouble codes” related to that sensor, Ford says it will replace the transmission lead frame for free. F-150 drivers can determine if their vehicle is impacted by entering their Vehicle Identification Number online on Ford’s recall webpage.

Source: Ford recalls 144,000 F-150s in Canada due to gearshift issue | CBC News

May He grant you according to your heart’s desire, And fulfill all your purpose.
Psalm 20:4

Hyundai recalls nearly 300K vehicles for seatbelt issue

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close up shot of a hyundai steering wheel

Nearly 300,000 Hyundai vehicles have been recalled due to a defect that could cause seat belt anchors to fail. According to the National Highway Traffic Safety Administration, the defective seat belt anchors in approximately 290,000 Hyundais could increase the risk of injury in a crash.

Four Hyundai models are impacted by the recall: Ioniq 6, the Genesis G-90, as well as the Santa Fe and Santa Fe Hybrid. The recall affects vehicles between model years 2023 and 2026. Hyundai dealers will inspect the seat belt anchors free of charge and replace them if necessary. Owners should receive letters in the mail about this in June. Owners can contact Hyundai customer service at (855)-371-9460 and be prepared to share the last four digits of their vehicle’s identification number.

Source: Hyundai recalls nearly 300K vehicles for seatbelt issue

Jesus Christ is the same yesterday, today, and forever.
Hebrews 13:8

Ford recalls 1.4 million F-150 pickup trucks

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pexels-photo-33336584.jpeg

Ford is recalling almost 1.4 million of its F-150 pickup trucks in the U.S. because of a gearshift issue that may lead to the loss of control of vehicles and increasing the risk of a crash. The automaker is aware of two injuries and one accident possibly related to the issue. Advertisement The recall includes F-150 light trucks with a six-speed automatic transmission that were produced between March 12, 2014 an Aug. 18, 2017. The National Highway Traffic Safety Administration’s safety recall report says that some of the pickup trucks may experience an intermittent selection signal of the transmission range sensor to the powertrain control module, which may lead to a temporary, unintended downshift into second gear.

This may cause an abrupt reduction in wheel speed for a short period of time, which in some situations could cause the rear tires to slide until the vehicle speed slows. Ford is aware of 444 warranty claims and 105 customer service reports that could be linked to the issue as of early this month. Vehicle owners will be notified about the recall by mail and instructed to bring their vehicle to a Ford or Lincoln dealer to have their powertrain control module calibration updated at no cost.

Source: Ford recalls 1.4 million F-150 pickup trucks

Then He said to them all, “If anyone desires to come after Me, let him deny himself, and take up his cross daily, and follow Me.”
Luke 9:23

Honda Recalls 440,830 Minivans Due to Airbag Malfunction Issue

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hands gripping car steering wheel close up

Honda Recalls 440,830 Minivans Due to Airbag Malfunction Issue AP Photo/David Zalubowski AMY FURR16 Apr 202614 Honda is recalling a large number of its Odyssey minivans due to an airbag problem that is linked to a software programming issue. The automaker is recalling 440,830 of the vehicles and said a software flaw could trigger side airbags to deploy unexpectedly when the vehicles encounter minor roadway issues such as speed bumps, increasing the risk for injury, Fox Business reported Thursday. Honda said there were 130 warranty claims and 25 reported injuries related to the problem.

The vehicles affected were the 2018 to 2022 models manufactured between late January 2017 and early June of 2022. Dealerships have said they will not charge owners to have the defect addressed and fixed. As of Thursday, owners can look up their vehicle identification numbers (VINs) on the National Highway Traffic Safety Administration (NHTSA) website, ABC 10 reported. “The recall is largely precautionary, with NHTSA estimating only about 0.1% of recalled cars will actually experience the airbag defect, ” the outlet said. “Honda began alerting dealers to the recall last Friday, and the car company expects to issue its notices to car owners on May 25.” The Fox article said safety regulators mentioned Honda may have been aware of the problem days before it was reported.

“Please be reminded that under Federal law, this agency is to be notified of all safety defect and/or noncompliance decisions within five business days. … Significant civil penalties can be assessed for this violation,” NHTSA said. In June, Honda recalled nearly 260,000 vehicles in the U.S. due to a faulty brake pedal that could raise the risk of a crash or injury,

Breitbart News reported: Reuters reports this recall affects specific models, including the 2021-2025 Acura TLX, 2023-2025 Acura MDX, and 2023-2025 Honda Pilot. Car owners are advised to stay informed about developments to ensure their safety on the road. There have been three warranty claims related to the recall and no reported injuries or deaths linked to the matter, according to the Japanese manufacturing giant. Months later, the automaker recalled over 400,000 of its Civics due to a wheel defect risk that could cause the wheels to fall off the cars, per WLTX.

Source: Honda Recalls 440,830 Minivans Due to Airbag Malfunction Issue

For with the heart one believes unto righteousness, and with the mouth confession is made unto salvation.
Romans 10:10

Batch of Anti-Anxiety Drug Xanax Recalled Over Safety Concerns

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Batch of Widely Used Anti-Anxiety Drug Xanax Recalled Over Safety Concerns Getty KATHERINE HAMILTON16 Apr 202652 1:37 A single lot of a widely used anti-anxiety drug called Xanax has been recalled, the U.S. Food and Drug Administration (FDA) announced. “The drug’s distributor, Viatris, said it was recalling one lot containing 51 bottles of 3 milligram extended release tablets because of concerns that they might not dissolve in the body as expected,” the New York Times reported. “This can affect how much of the drug is released and absorbed over time, making the effects less predictable.

The pills were sold nationwide under the brand name Xanax XR.” The company said it has not received any reports of adverse events and that the “risk to the patient associated with this event is considered to be negligible.”  Viatris said the recalled pills were in 60-pill bottles between August 2024 and May 2025. The lot number is 8177156 with an expiration date of Feb. 28, 2027, according to the report. A spokesman for Viatris said the recall is for pharmacies so they can remove the lot from store shelves. The spokesperson said “patients do not need to take any action.” Xanax is a benzodiazepine prescribed to treat anxiety and panic disorder and can be highly addictive.

Source: Batch of Anti-Anxiety Drug Xanax Recalled Over Safety Concerns

That I may come to you with joy by the will of God, and may be refreshed together with you.
Romans 15:32

‘Hazardous’: Nail polish remover sold on Amazon recalled

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a person applying a nail polish

Thousands of bottles of nail polish remover sold on Amazon have been recalled after hazardous substances that are “strictly prohibited” were detected in the product, according to the U.S. Food and Drug Administration. The Morovan gel nail polish remover was found to have methylene chloride and chloroform in it, which officials said “is a concern because it has been shown to cause cancer in animals and is likely harmful to human health.” Methylene chloride is a prohibited ingredient in the U.S. and “is not allowed in cosmetics at any level under FDA regulations,” according to the FDA. Anyone who purchased the nail polish remover was urged to stop using it “immediately,” label the bottle with the word “recalled” on it and safely dispose of it. The company asked customers to then submit a photo of the disposal. “Following proper disposal, kindly take a photograph of the discarded product (clearly showing the ‘Recalled’ label and the product itself) and submit the image via email to our customer service team for verification,” the company wrote in its recall notice. “The designated email address for submission is: customer-service@morovan.com.” According to Morovan, about 4,000 bottles were included in the recall.

Source: ‘Hazardous’: Nail polish remover sold on Amazon recalled – NBC Chicago

The grace of our Lord Jesus Christ be with you all. Amen.
Revelation 22:21

More than 350,000 vitamins and supplements recalled over poisoning risk

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More than 350,000 bottles of iron-containing dietary supplements sold nationwide have been recalled after investigators found they posed a serious poisoning risk. Manufacturer Vitaquest International, which is behind brands including Bari Life, Arey and NuLife, issued the alert after finding the supplements’ packaging was not child-resistant. Health officials warned that this could lead to children accidentally overdosing, causing serious injury or even death. The affected supplements were sold between April 2023 and February 2026 for between $13 and $130 per bottle.  They were available at retailers including Erewhon, Vitamin Shoppe and Amazon. The brands the iron supplements were sold under include Arey, Bari Life, Bird&Be, Biote, Dr. Fuhrman, NuLife, HMR, Bariatric Pal, Noevir, Zenbean and Sakara. No injuries or illnesses have been reported to date.

Source: More than 350,000 vitamins and supplements recalled over poisoning risk | Daily Mail Online

A new commandment I give to you, that you love one another; as I have loved you, that you also love one another.
John 13:34

GM recalls more than 270,000 cars in U.S. over rearview camera risk

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General Motors is recalling more than 270,000 vehicles in the U.S. over a problem with their rearview cameras. The cameras on certain 2023-2025 Chevrolet Malibu vehicles may display blank or distorted images, posing a risk to drivers, according to a filing with the National Highway Traffic Safety Administration (NHTSA). “A rearview image that does not display correctly reduces the driver’s view behind the vehicle, increasing the risk of a crash,” the safety alert notes.

Only about 6% of the vehicles under recall have faulty cameras, according to the recall report. GM’s camera supplier, Sharp Electronics, identified an issue with the bonding process used to build the camera housing that could weaken the adhesive material on some assemblies.  GM also found that the mounting configuration of the Sharp camera on the Chevrolet Malibu could expose it to moisture that may penetrate the housing. The automaker indicated it is not aware of any crashes or injuries associated with the defect. GM will mail letters to owners of potentially affected vehicles on May 18, according to NHTSA. Owners can bring their cars to GM dealerships, which will replace the rearview cameras free of charge.

Source: GM recalls more than 270,000 cars in U.S. over rearview camera risk – CBS News

Therefore, my beloved brethren, be steadfast, immovable, always abounding in the work of the Lord, knowing that your labor is not in vain in the Lord.
1 Corinthians 15:58

Graco infant car seats sold at Amazon, Target and Walmart recalled over structural issue

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empty child car seat in modern vehicle interior

Graco is voluntarily recalling select infant car seats due to a “structural issue” with the base, the company announced. The recalled SnugRide Turn & Slide seats were sold in the U.S. from Jan through March 2026 at Amazon, Babylist, Target, Walmart, and on Graco’s website. “We know parents rely on Graco products every day, and we understand this may create frustration and disruption for families,” Graco said. “We are working quickly to support affected families and will provide a replacement product at no cost.” Which car seats are included in Graco’s recall? You’ll need to check the model number and color of the seats, according to Graco. This can be found on the product label. In addition to verifying with the below list of recalled models, you can enter the seat’s model number on Graco’s website to confirm whether it has been recalled. When is Target’s 2026 car seat trade-in, and what will you receive?

The recalled products include the following products with the matching model numbers and colors:

  • Noir/Black 2231887
  • Sandstone/Tan 2231806
  • Mulberry/Girl-Plum 2231885
  • Sandstone/Tan 2231881
  • Noir/Black 2231884
  • Noir/Black SnugRide Turn & Slide Rotating Infant Car Seat Base: 2231810
  • Black Modes Nest Travel System with SnugRide Turn & Slide ICS: 2243083 Noir/Black
  • SnugRide Turn & Slide Rotating Infant Car Seat: 2231809

What to do with the recalled car seat Graco advises customers to stop using the seat with the base immediately. They should take a photo of the product and upload it to gracobaby.com/nsrecall/recall.html for a replacement. “The current seat may continue to be used without the base in accordance with the product instructions while you wait for your selected replacement product,” Graco said.

Source: Graco infant car seats sold at Amazon, Target and Walmart recalled over structural issue

I set My rainbow in the cloud, and it shall be for the sign of the covenant between Me and the earth.
Genesis 9:13

Ford recalls nearly 423,000 vehicles over windshield wiper issue

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man checking the engine of a car

Ford Motor Co. is recalling 422,613 vehicles because the windshield wipers might fail, according to a notice from the National Highway Traffic Safety Administration (NHTSA). The agency said the failure could reduce the driver’s visibility and increase the risk of a crash. The recall affects Lincoln Navigator and Expedition vehicles, as well as some of Ford’s F-Series trucks. 

Vehicles included in recall:

  • 2021-2023 Lincoln Navigator vehicles
  • 2021-2023 Expedition vehicles
  • 2022-2023 F-250 SD vehicles
  • 2022-2023 F-350 SD vehicles
  • 2022-2023 F-450 SD vehicles
  • 2022-2023 F-550 SD vehicles
  • 2022-2023 F-600 vehicles

Ford plans to send a letter to affected owners on April 13, 2026, to notify them of the windshield wiper issue and corresponding safety risks. Owners can take their vehicles to a dealership to have the wipers replaced free of charge, NHTSA said. Ford’s recall number is 26S24.

Source: Ford recalls nearly 423,000 vehicles over windshield wiper issue – CBS Sacramento

For if when we were enemies we were reconciled to God through the death of His Son, much more, having been reconciled, we shall be saved by His life.
Romans 5:10

Wawa recalls 4 popular drinks after allergen contamination

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According to the FDA, Wawa recalled the drinks after workers found an issue with equipment that may have led to the possibility of a milk allergen in the products.

The four drinks impacted are the 16oz versions of:

Wawa Iced Tea Lemon
Wawa Iced Tea Diet Lemon
Wawa Diet Lemonade
Wawa Fruit Punch
All of the recalled products have been taken off of store shelves but if you bought any of these drinks recently, you should throw them out.

The FDA says that no one has reported any illnesses because of the potential contamination.

Wawa drinks recalled
Wawa Iced Tea Lemon in 16 oz Pint bottles

UPC: 726191018425 
Code Date: MAY 15, 2026
Sold in 123 stores in Del., Md., NJ, Pa. and Va.
Wawa Iced Diet Tea Lemon in 16 oz Pint bottle

UPC: 726191018548
Code Date: MAY 18, 2026 
Sold in 8 stores in NJ and Pa.
Wawa Diet Lemonade in 16 oz Pint bottles

UPC: 726191055901
Code Date: May 18, 2026 
Sold in 12 stores in Del. and NJ
Wawa Fruit Punch in 16 oz Pint bottles

UPC: 726191018432
Code Date: May 19, 2026 
Sold in 53 stores in Del., Md., NJ, Pa. and Va.

Source: Wawa recalls 4 popular drinks after allergen contamination – NBC10 Philadelphia

Do not overwork to be rich; Because of your own understanding, cease!
Proverbs 23:4

Hyundai recalls some Canadian vehicles due to seatbelt issue

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close up on hyundai steering wheel

Hyundai is issuing a warning related to the seatbelt system in some of its 2026 Palisade models. In some cars, wiring in the seatbelt for the third-row, left-hand side seat can become damaged when pulled, according to a notice on Transport Canada’s Motor Vehicle Safety Recalls Database. The wiring issue can then cause the seatbelt indicator to show that the seatbelt is buckled when it is not. “A seatbelt status indicator that doesn’t work correctly could create confusion. Not wearing a seatbelt increases the risk of injury in a crash,” the notice said.

Some 4,203 vehicles in Canada may be affected by the seatbelt issue. Hyundai says it will notify affected drivers of the issue in writing and advise them to visit a dealership to have the seatbelt wiring fixed. Alternatively, drivers can input their vehicle identification number in Hyundai’s online recall lookup website to see if their car is impacted, or call 1-888-216-2626. Earlier this year, Hyundai recalled thousands of vehicles in the U.S. and Canada and stopped sales of some of its new Palisades due to a different issue that caused some second and third-row power seats not to stop moving when they detected contact with a passenger or an object.

Source: Hyundai recalls some Canadian vehicles due to seatbelt issue | CBC News

For if you forgive men their trespasses, your heavenly Father will also forgive you.
Matthew 6:14

California dairy recalls raw milk cheese linked to severe strain of E. coli

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Raw Farm is recalling its raw milk cheddar cheeses amid an outbreak of a dangerous strain of E. coli, according to the Food and Drug Administration.

As of Friday, the FDA reported that the cheeses are linked to nine people in three states who developed E. coli O157:H7, a severe type of the bacteria that can cause stomach cramps, vomiting and bloody diarrhea. The cases are in California, Texas and Florida.

The California dairy company previously refused to recall its products when the FDA’s investigation began in mid-March.

Three people have been hospitalized and one person developed hemolytic uremic syndrome, a life-threatening E. coli complication that can cause kidney failure. Over half of the illnesses are in children under 5 years old. No deaths have been reported.

To find a potential link, the FDA interviewed eight of the infected people about what they ate the week prior to infection. All of them reported eating raw dairy products.

The FDA is testing samples for E. coli, but hasn’t confirmed a positive test result so far. Raw Farm President Aaron McAfee said that won’t happen.

“We’re not related to this outbreak,” he said.

McAfee said the voluntary recall was “made under protest” and “simply a moment in time where this was the right decision for Raw Farm and our consumers.”

“RAW FARM continues to contest the epidemiological links provided by the FDA,” the company said in a statement released Thursday.

Raw milk products are made from dairy that hasn’t been pasteurized, a process that heats it enough to destroy bacteria.

Source: California dairy recalls raw milk cheese linked to severe strain of E. coli

Blessed be the God and Father of our Lord Jesus Christ, the Father of mercies and God of all comfort, who comforts us in all our tribulation, that we may be able to comfort those who are in any trouble, with the comfort with which we ourselves are comforted by God.
2 Corinthians 1:3-4

Eye drops sold at Walgreens, CVS recalled over safety concerns, FDA says

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A pharmaceutical company has issued a voluntary recall of over 3 million of its over-the-counter eye-drop products after the Food and Drug Administration cited a “lack of assurance of sterility.”

According to the FDA notice, K.C. Pharmaceuticals, of Pomona, California, manufactures the products for a number of brands sold under names such as “Dry Eye Relief Eye Drops,” “Sterile Eye Drops” and “Artificial Tears Sterile Lubricant Eye Drops.” The recall of 3,111,072 bottles began in early March.

The eye drops are sold at major retailers, including CVS, Walgreens and Rite Aid.

There aren’t reports of injuries associated with the eye drops yet. The FDA notice classified the action as a “Class II recall.” Class II recalls apply to products that can cause “temporary or medically reversible” health problems.People can continue using their medication during a Class II recall unless stated otherwise by the company, according to the FDA.

Source: Eye drops sold at Walgreens, CVS recalled over safety concerns, FDA says

But the fruit of the Spirit is love, joy, peace, longsuffering, kindness, goodness, faithfulness, gentleness, self-control. Against such there is no law.
Galatians 5:22-23

Nearly 90,000 bottles of children’s ibuprofen recalled due to reports of foreign substances

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A pharmaceutical company issued the recall after receiving complaints of “gel-like mass and black particles” in the product, the FDA said.

Source: Nearly 90,000 bottles of children’s ibuprofen recalled due to reports of foreign substances – CBS Atlanta

For the wages of sin is death, but the gift of God is eternal life in Christ Jesus our Lord.
Romans 6:23