Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Over 93,000 cases of Arctic Shores frozen raw shrimp have been recalled due to potential contamination with Cesium-137. The shrimp were manufactured under insanitary conditions that raise serious health concerns. Consumers should not consume this product and should seek a refund from Great American Seafood Imports.
Biomet recalled 98 ZipTight Acute AC Joint Implant Single Ziploop devices on Sept. 23, 2025. A missing slotted button assembly was identified in one lot. Healthcare providers and patients should stop using the device immediately and follow Biomet’s recall instructions.
Southwind Foods LLC dba Great American Seafood Imports Co. expanded recall covers Arctic Shores, Best Yet, Great American and Master Catch frozen shrimp sold nationwide by multiple retailers after Cesium-137 contamination was detected. The contaminated product was manufactured under insanitary conditions. Consumers should not eat the product and should contact the company for refunds or replaced.
BD recalled 4,283 Phoenix M50 Automated Microbiology Systems worldwide after unauthorized access to product service credentials. The unauthorized actor could access affected products and data. Labs should stop using these devices and follow the recall instructions from BD; contact BD for remediation guidance.
BD recalled 177 units of the BACTEC Blood Culture System worldwide after an unauthorized actor accessed product service credentials. The breach could allow unauthorized access to system configurations and data. Healthcare facilities should stop using the affected equipment and follow BD’s recall instructions.
OptiWize Health recalled 78 units of its Collagen Plus supplement on September 23, 2025. Testing revealed discrepancies in labeled ingredient quantities, particularly lower manganese levels. Consumers should not consume the product and contact the company for refunds.
BD recalled 1,086 BD BACTEC Blood Culture System units worldwide after unauthorized access to product service credentials. The breach could compromise confidentiality, integrity and availability of affected devices and data. Hospitals and healthcare providers should stop using the device immediately and follow BD’s recall instructions.
El Rojo Wholesale recalled 2,904 units of El Rojo Pasta De Harina, Wheat Pellets, distributed in Minnesota. The recall cites missing ingredient information and no nutritional panel. Consumers should not eat the product and should contact the company for refund or replacement.
BD recalled 38 Veritor Connect Software units distributed to healthcare providers worldwide. Unauthorized access to product service credentials could affect confidentiality, integrity or availability of the product and data. Stop using the software and follow the recall instructions provided by the manufacturer.
Great American Seafood Imports recalled 93,122 cases of its frozen raw shrimp skewers after potential Cs-137 contamination. The recall expansion cites insanitary manufacturing conditions. Consumers should not consume the product and should contact the company for refund or replacement.
BD recalled 2,050 units of the EpiCenter Microbiology Data Management System due to unauthorized access to product service credentials. The defect could allow access to confidential data. Stop using affected devices and follow manufacturer guidance for updates or replacement.
Arctic Shores recalled 93,122 cases of Frozen cooked salad shrimp in 6 oz bags. The recall affects products distributed to 26 states. The product may be contaminated with Cesium-137 due to insanitary manufacturing conditions. Consumers should not eat this product and should contact Southwind Foods LLC dba Great American Seafood Imports for refund or replacement information.
Tengen USA Trading Corp recalled YO!MAN Lettuce (Spicy Flavor) on September 23, 2025. The product contains undeclared cyclamates, posing health risks. This recall affects 26 cases distributed across several states, including New York and Texas.
Tengen USA Trading Corp recalled 26 cases of YO!MAN Cucumber (Fresh Hunan Flavor) on September 23, 2025, due to undeclared cyclamates. The product poses a high risk of poisoning for consumers allergic to this chemical. Consumers should not consume the product and seek refunds.
RC Outsourcing recalled 2,669 bevacizumab intravitreal syringes distributed nationwide to hospitals and clinics. The recall cites a lack of assurance of sterility. Stop using the product immediately and contact RC Outsourcing or your healthcare provider for guidance. Recall notices will be sent by letter.
Sea Port brand Raw Frozen Easy Peel Headless Shell-On White Shrimp, Jumbo 16-20, distributed by Sea Port Products Corp in Kirkland, WA, is recalled. A Cs-137 contamination risk is identified. About 1,800 cases are affected across two master-case configurations. Consumers should not consume the product and should contact Sea Port for refunds or replacements.
Ascend Laboratories recalled Atorvastatin Calcium Tablets USP 40 mg, 90-count (NDC 67877-513-90), 500-count (NDC 67877-513-05), and 1,000-count (NDC 67877-513-10) nationwide in the United States. The batches failed dissolution specifications. Patients should stop using the medication and contact Ascend Laboratories, LLC or their healthcare provider for guidance.
Black Sheep Egg Company recalls 58,500 dozen free range Grade AA medium brown eggs after FDA enforcement notice citing potential Salmonella contamination. The recall covers eggs sold in Arkansas and Missouri, with wholesale and broker locations in Mississippi, Texas, California and Indiana. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refund or replacement.
Black Sheep Egg Company recalled 46,800 dozen Free Range Grade AA Medium White Eggs sold at retail and wholesale outlets in Arkansas and Missouri. The FDA recall cites potential Salmonella contamination. Consumers should not consume the eggs and should contact Black Sheep Egg Company for refund or replacement.
Ascend Laboratories, Parsippany, NJ is recalling 141,984 bottles of ATORVASTATIN CALCIUM Tablets USP, 10 mg, nationwide, manufactured by Alkem Laboratories, Ltd. in India. The issue is failed dissolution specifications, which could lead to improper dosing. Healthcare providers and patients should stop using the product and contact Ascend Laboratories for guidance.