Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Pacific Coast Producers recalled 1,836 cases of Pears Halves in Pear Juice from Concentrate distributed by Walmart. The product may be contaminated with lead, a heavy metal hazard. Consumers should not eat this product and should contact Pacific Coast Producers for a refund or replacement by telephone.
American Contract Systems recalled 32,433 cardiac cath lab kits distributed nationwide to healthcare providers. The devices were re-gassed after a nonconformance in the Ethylene Oxide gas injection process. The kits have not been validated for exposure to multiple sterilization cycles and cannot be guaranteed safe.
American Contract Systems recalled 32,433 radiology packs after a nonconformance during EO gas injection. The items were re-gassed and not validated for multiple sterilization cycles. The recall is active as of 2025-10-22. US distribution included SD, IA, MN, WA, IL. Health risks prompt immediate removal from use.
American Contract Systems recalled 32,433 medical convenience kits nationwide in the United States after re-gassing sterilization cycles. The recall covers multiple packs including HEART PACK and PACEMAKER PACK with 2025 recall date. The safety issue centers on EO gasset validation failures after a nonconformance during initial gas injection. Stop using immediately and follow recall instructions.
Gospodarstwo Pasieczne Sadecki Bartnik recalled 336 jars of Bee Pollen sold in Illinois after tests detected pyrrolizidine alkaloids. The product contains detectable pyrrolizidine alkaloids. Consumers should not consume the product and should contact the producer by telephone for refund or replacement.
ONE FROZEN recalled 57,240 bags of Good and Gather Southwest-Style Burrito Bowl Blend sold nationwide after discovering undeclared shrimp. The product may contain shellfish due to cross-contact risk in a facility that also handles shellfish and other allergens. Consumers should not eat the product and should contact ONE FROZEN for a refund or replacement.
Pacific Coast Producers recalled 102 cases of Halved Pears in Pear Juice Concentrate sold nationwide through Wegmans distribution after detecting potential lead contamination. The product is packaged in 15-ounce cans with Lot 6PJ 09 C2295 and UPC 077890747490. Consumers should stop using the product and contact Pacific Coast Producers for refund or replacement.
American Contract Systems recalled 32,433 Basic Biopsy Trays nationwide after discovering re-gassing occurred following a nonconformance during Ethylene Oxide sterilization. The trays have not been validated for exposure to multiple sterilization cycles, so product quality and safety cannot be confirmed. Healthcare providers and patients should stop using the device immediately and follow theメーカー?
Pacific Coast Producers recalled 203 cases of Pears Sliced in Organic Pear Juice from Concentrate distributed by Wegmans Food Markets. The products may be contaminated with lead. Consumers should not eat them and should contact Pacific Coast Producers by telephone for refund or replacement.
Pacific Coast Producers recalled 609 cases of Fruit Cocktail in 15 oz cans distributed by Wegmans Food Markets over lead contamination concerns. The recall cites potential contamination with lead. Consumers who purchased the product should not consume it and should contact Pacific Coast Producers for a refund or replacement.
American Contract Systems recalled 32,433 basic biopsy trays distributed nationwide in the United States. These trays were re-gassed after a nonconformance occurred during the initial Ethylene Oxide gas injection. The trays have not been validated for exposure to multiple sterilization cycles. Healthcare providers and patients should stop using affected trays and follow recall instructions.
American Contract Systems is recalling 32,433 medical Angio Packs distributed nationwide in the United States. The devices were re-gassed after a nonconformance in the Ethylene Oxide gas injection process. Healthcare facilities and patients should stop using the devices and follow the manufacturer’s recall instructions.
American Contract Systems recalled 32,433 medical convenience kits after it was discovered they were re-gassed after sterilization failure. The sterilization process may compromise the product's quality, safety, and effectiveness. Healthcare providers must stop using these kits immediately and follow up with the manufacturer for instructions.
American Contract Systems recalled 32,433 labor and delivery packs nationwide in the United States, including the states of South Dakota, Iowa, Minnesota, Washington and Illinois. Re-gassing occurred after a nonconformance in the Ethylene Oxide gas injection process. The affected packs have not been validated for exposure to multiple sterilization cycles. Hospitals and health systems should stop使用
American Contract Systems recalled 32,433 medical convenience kits sold through multiple retailers nationwide. The devices were re-gassed after a nonconformance in the Ethylene Oxide gas injection process and have not been validated for exposure to multiple sterilization cycles. Healthcare providers and patients should stop using these products immediately and follow the manufacturer's recall.
American Contract Systems recalled 32,433 UDPG88W PICC G-TUBE PACK medical kits nationwide after a nonconformance in Ethylene Oxide sterilization led to re-gassing. The devices have not been validated for multiple sterilization cycles. Healthcare providers and patients should stop using the kit immediately and follow recall instructions.
Philips Medical Systems Nederland B.V. recalls 2,114 Allura Xper FD20 imaging systems sold worldwide after reports that internal components may deteriorate. The recall covers models 722012, 722028 and 722006 with associated 510(k) numbers K102005 and K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949. If deterioration occurs, motorized movements may fail. Manual and imaging功能s,
Philips Medical Systems Nederland B.V. recalled 268 Allura Xper FD20 Biplane imaging systems worldwide, including 102 in the United States. The recall cites deterioration of internal components that could disable motorized movements. Hospitals should stop using the devices immediately and follow the manufacturer’s recall instructions.
Zydus Lifesciences and Zydus Pharmaceuticals US recall Chlorpromazine Hydrochloride Tablets, 10 mg, 100-count bottles sold nationwide in the United States after detecting an impurity above acceptable intake. The impurity is N-Nitroso Desmethyl Chlorpromazine. Consumers should stop using the product immediately and contact the manufacturer for guidance.
Philips Medical Systems Netherlands B.V. recalls 1,117 Allura Xper FD10 imaging systems worldwide, including 252 units in the United States. The defect involves deterioration of internal components such as the CMOS battery, hard disk drive and power supply unit, which can disable motorized movements. Hospitals should stop using the devices and follow the manufacturer recall instructions.