1,003 recalls tagged with “chemical hazard”.
Medline Industries recalled 41 lots of reprocessed electrophysiology catheters on December 22, 2025. These devices may contain residual material that poses serious health risks. The recall affects several specific model numbers and follows the expansion of a previous recall.
DPT Laboratories recalled 92,376 tubes of Diclofenac Sodium Topical Gel, 1%, on December 22, 2025. The recall is due to the product failing pH specifications, posing a high risk to consumers. Users should stop using the gel immediately and contact healthcare providers for guidance.
Baxter Healthcare Corporation recalled 125,496 bottles of Sterile Water for Irrigation on December 22, 2025. Plastic particles from the bottle rim contaminated the solution, posing a health risk. Consumers and healthcare providers must stop using the product immediately and seek guidance.
Willy Pete's Chocolates recalled 54 units of Almond Despair dark chocolate on December 22, 2025. The product contains undeclared almonds which pose a risk to consumers with nut allergies. Customers should stop using the product and seek a refund or replacement.
Atwater's recalled 197 Holiday Cookie Tins on December 21, 2025. The tins contain undeclared tree nut allergens including almonds, pecans, and walnuts. Consumers should not consume the product and seek refunds.
Novo Nordisk recalled Wegovy (semaglutide) injections on December 19, 2025, after discovering hair in prefilled syringes. The contamination poses a serious hazard to consumers. The recall affects all units distributed nationwide.
Novo Nordisk recalled Wegovy (semaglutide) Injection on December 19, 2025, due to hair found in a prefilled syringe. The recall affects products distributed nationwide in the United States. Consumers should stop using the product immediately and contact their healthcare provider.
Sato Pharmaceutical Co., Ltd. recalled 3,640 bottles of INON ACE Antacid tablets on December 19, 2025. The recall follows failed disintegration specifications, indicating the tablets may not dissolve properly. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Gregory's Foods recalled 308 cases of White Chocolate Macadamia Nut frozen cookie dough on December 19, 2025. The product contains undeclared peanuts, posing a serious allergy risk. Consumers should not consume the product and seek refunds.
Bisaf Strep A Self-Test from Altruan GmbH remains active in recall status after the FDA flagged lack of clearance. The Class II medical device was distributed nationwide in the United States. The hazard is lack of FDA clearance. Consumers should stop use immediately and follow manufacturer guidance.
ICU Medical has recalled over 14 million needle-free access devices after reports of fluid leaks and potential exposure to biological contaminants. The recall affects devices distributed worldwide, including in 50 states and multiple countries. Users must stop using these devices immediately and follow recall instructions from the manufacturer.
Zydus Pharmaceuticals recalled over 2,100 bottles of TraZODONE Hydrochloride Tablets on December 19, 2025. Some tablets have surface dents that may affect medication integrity. Consumers should stop using the product immediately and seek guidance from healthcare providers.
CATAO MARKET recalled 520 master cases of its Authentic Cuban Loaf Cake Raisins on December 18, 2025. The recall occurred due to undeclared FD&C Yellow #5, which poses a high allergy risk. The affected products were distributed only in Florida and have best by dates from December 18, 2025, to March 18, 2026.
CATAO MARKET recalled 385 master cases of Mini Gaceniga Authentic Cuban Loaf Cake on December 18, 2025. The recall occurred due to undeclared FD&C Yellow #5, which poses a health risk to sensitive individuals. Consumers in Florida should stop using the product immediately and seek a refund.
Imprimis NJOF, LLC recalled 778 boxes of Dexamethasone Moxifloxacin intraocular injection on December 18, 2025. The recall stems from the presence of glass-like particles in the product. Consumers and healthcare providers should stop using the product immediately.
Waterfront BISTRO brand Frozen Raw Shrimp was recalled on December 18, 2025, due to possible contamination with Cesium-137. Approximately 1,800 cases of the product are affected. Consumers should not consume the shrimp and seek a refund or replacement.
Feel The Beard recalled its minoxidil beard growth serum on December 18, 2025, due to a serious poisoning risk. The packaging fails to meet child-resistant requirements, which could lead to severe injury or death if ingested by young children. Consumers must stop using the product immediately and contact the company for further instructions.
Plantimex recalled Mamisan Pain Relieving Topical Ointment on December 18, 2025. The ointment's packaging does not comply with child-resistant standards, posing a serious poisoning risk to children. Consumers should stop using the product immediately and secure it out of children's reach.
CATAO MARKET recalled 3,120 Cuban loaf cakes on December 18, 2025. The recall follows the discovery of undeclared FD&C Yellow #5 in the product. This hazard poses a significant risk for consumers with allergies to this color additive.
Price Chopper recalled 3,290 cases of frozen raw shrimp on December 18, 2025. The shrimp may be contaminated with Cesium-137, a radioactive isotope. Consumers should stop using the product and seek refunds.