All articles tagged with #recall
The FDA issued a Class II recall of about 2.5 million bottles of prednisolone acetate ophthalmic suspension 1% eye drops by Lupin Pharmaceuticals due to a potential foreign-substance contamination. The products—available in 5 mL, 10 mL, and 15 mL sizes—were initially recalled on June 4 and reclassified on June 30; the drops treat non-infectious eye allergies and inflammation.
The FDA has recalled more than 2.5 million bottles of Lupin's prednisolone acetate eye drops due to a possible foreign substance; the substance and its entry method aren’t identified. The affected bottles (5 mL, 10 mL, 15 mL) are from India-based Lupin and are used to reduce inflammation after eye surgery or for allergies. Because this is a Class II recall (high risk), patients should not stop using the product on their own and should consult an eye doctor or pharmacist for guidance based on their condition.
Kao USA is recalling Oribe Serene Scalp Densifying Shampoo sold nationwide after the FDA detected Pluralibacter gergoviae; the affected products (8.5 oz and 33.8 oz) were manufactured Feb 21–26 in lots starting with YR. While the bacteria pose little risk to healthy people, those with weakened immune systems may be more vulnerable. Consumers should contact Kao’s Professional Hair Hotline at 800-333-2442 or [email protected] for a replacement.
Shampoo produced and sold nationwide by Kao USA (Oribe Serene Scalp Densifying Shampoo in 8.5 oz and 33.8 oz sizes) is recalled after the FDA found Pluralibacter gergoviae contamination; affected products manufactured Feb. 21–26 with lot codes starting with YR. Consumers should contact Kao at 800-333-2442 or [email protected] for a replacement.
Publix is recalling GreenWise Organic IQF Blueberries (10-ounce) produced by Frutas y Hortalizas del Sur S.A. and distributed to eight states after 12 people reported E. coli O145 illnesses; the affected lot is 60401 with a best-by date of Feb 9, 2028. Shoppers who bought the product should discard it or return it for a refund; no other lots are affected. The recall covers Alabama, Florida, Georgia, Kentucky, North Carolina, South Carolina, Tennessee, and Virginia; the supplier is investigating the contamination source.
The FDA has elevated Utz Quality Foods' recall of Zapp’s and Dirty potato chips to Class 1, its highest risk level, after a seasoning containing dry milk powder may be contaminated with Salmonella. The issue, tied to a supplier from California Dairies, Inc., prompted recalls announced April 28 and affects a limited number of products; no illnesses have been reported. Consumers should discard affected products and contact Utz for refunds; other Utz items are unaffected.
Conair is recalling about 1.72 million Cuisinart metal-wire grill brushes after reports that bristles can detach and be ingested, risking internal injuries. The recall covers multiple models sold from 2009–2026. Consumers should stop using the recalled brushes, contact Conair for a full refund or credit (plus 20% of the refund), and discard the brushes. There have been at least 54 reports of bristle detachment, including three ingestion cases.
During a Memorial Day barbecue in Stillwater, Minnesota, a teen unknowingly swallowed a metal grill-bristle buried in a burger. A week later it punctured his intestine, forcing emergency bowel surgery via a six-inch abdominal incision, as recalls of millions of metal grill brushes for ingestion hazards highlight the danger.
FDA upgraded Utz’s recall of Zapp’s and Dirty potato chips to Class 1 due to possible salmonella contamination from a dry milk powder seasoning ingredient; about 650,000 bags with best-by dates from late July to late August are affected. Utz reports no illnesses and urges consumers to discard the products and seek refunds; the agency has not provided further details on the consumer risk.
The FDA has issued a Class I recall—the highest risk level—for more than 650,000 bags of Zapp’s and Dirty-brand potato chips after a seasoning containing dry milk powder potentially contaminated with salmonella was used; Utz reports no illnesses and is offering refunds, while retailers have removed affected products from shelves. Consumers should discard recalled chips, check best-by dates and batch codes, and contact Utz for refunds as part of a broader investigation into the ingredient.
The FDA has upgraded the recall of certain Zapp's and Dirty Brand potato chips to Class I, the highest risk level, due to possible salmonella contamination; initially announced by Utz Quality Foods in May, the affected products span several flavors and sizes, and consumers should discard them and not eat them.
Ford is recalling 741,195 U.S. vehicles over a transmission defect that can damage the park system and let a vehicle roll away; affected models include 2018–2021 Navigator, Expedition, 2020–2021 Explorer, Lincoln Aviator, and 2021 F-150, with dealers updating software and replacing damaged transmission components at no charge. Separately, Ford is recalling 36,046 Broncos for improperly secured fender flares that can detach and pose a crash risk; dealers will inspect and repair or replace flares at no cost.
Nearly 1 million bottles (about 944,142) of Amgen medications Corlanor (ivabradine) and Sensipar (cinacalcet) have been recalled nationwide after foreign matter was found on the exterior surface of tablets in a reserve sample. The issue was localized to the coating and occurred in bottles packaged in AML Building 23; the recalls cover multiple dosages and bottle counts distributed from Oct 28, 2021 to Dec 30, 2025. The FDA classified the recall as Class II with low overall patient-safety risk, and there have been no reported complaints.
Toyota is recalling 20,991 electric vehicles across the bZ, Solterra, and Lexus RZ lines due to a potentially faulty battery ECU that could cause a loss of power and increase crash risk. Dealers will update the battery ECU at no cost, with notification letters to be mailed around August 3, 2026. Models affected include 11,495 bZ, 4,757 Solterra, and 4,739 Lexus RZ, all built on the e-TNGA platform; other Toyota, Subaru, and Lexus EVs are not affected.
FSIS announced a recall of about 5,300 pounds of Molly’s Kitchen California Style Pasta Salad from Reser’s Fine Foods due to misbranding and undeclared allergens (egg and milk); the product may actually be chicken salad. It was produced on June 11, 2026 and shipped to distributors in Alabama, Florida, North Carolina, New Jersey, South Carolina, Tennessee, and Virginia for foodservice. No adverse reactions have been reported; consumers should discard the product or return it to the place of purchase. For questions, contact Reser’s Fine Foods Consumer Affairs or FSIS recall information on the FSIS website.