2,679 recalls tagged with “immediate action”.
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.
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 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.
DEMERS FOOD GROUP recalled 966 cases of Scott & Jon's Honey Sesame Salmon Rice Bowl distributed across nine states. The undeclared wheat allergen could trigger a reaction in wheat-allergic individuals. Consumers should not eat this product and should contact DEMERS FOOD GROUP for refunds or replacements.
Southwind Foods LLC, doing business as Great American Seafood Imports, recalled 93,122 cases of Tovala-brand frozen raw phosphate-free shrimp after identifying potential Cesium-137 contamination. The recall expands a prior action and notes insanitary production conditions. Consumers who bought the 5 oz IQF bag with UPC 829944085788 should not eat it and should contact the supplier for refund or re
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.
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.
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.
BD MAX System recall affects 62 units distributed worldwide in 2025 after unauthorized access to service credentials. An unauthorized actor accessed credentials used by BD technical support teams. Healthcare providers should stop using the devices and follow the manufacturer’s recall instructions.
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.
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.
Black Sheep Egg Company is recalling 288,900 dozen Free Range Grade AA Large Brown Eggs sold at retail and wholesale locations in Arkansas and Missouri, with broker distribution in Mississippi, Texas, California and Indiana. The recall cites potential Salmonella contamination as the hazard. Consumers should not consume these eggs and should contact Black Sheep Egg Company for refund or replacement
Black Sheep Egg Company recalled 20,625 dozen eggs sold at retail and wholesale locations in Arkansas and Missouri after a potential Salmonella contamination. The eggs are Free Range Grade AA Large Brown, loose-packed in boxes. Consumers should not consume these eggs and should contact Black Sheep Egg Company for refunds or replacements.
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 14,220 dozen Free Range Grade AA Medium Brown Eggs after FDA notice of potential Salmonella contamination. The recall covers loose-pack boxes sold at retail and wholesale locations in Arkansas and Missouri, with wholesale distribution to Mississippi, Texas, California and Indiana. Consumers should not consume the eggs and should contact the company for refunds or替换
Beckman Coulter recalled 571 DxI 9000 Access Immunoassay Analyzers and DxC 500i Clinical Analyzers distributed worldwide. A software anomaly may prevent correct application of manual dilution factors for tests already in progress on the same Sample ID. Labs should stop using the devices immediately and follow recall instructions.
Kico Knee Innovation recalls 21 ARVIS Shoulder systems nationwide after reports that AI planning software may cause implant malalignment or reduced range of motion. The recall covers software version V2025.1.2 used with IN-27300 hardware. Healthcare providers and patients should stop using the device and follow manufacturer instructions.