Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Tovala recalled 93,122 cases of frozen shrimp on September 23, 2025. The product may have been contaminated with Cesium-137. Consumers should stop using the product immediately and seek a refund.
Becton Dickinson & Co. recalled 2,050 units of its EpiCenter Microbiology Data Management System on September 23, 2025. Unauthorized access to product service credentials may compromise patient data. The recall affects models distributed worldwide, including the U.S. and Puerto Rico.
Southwind Foods LLC recalled 93,122 cases of frozen raw shrimp on September 23, 2025. The products may contain Cesium-137 due to insanitary manufacturing conditions. Consumers should not consume this shrimp and seek refunds immediately.
Southwind Foods LLC recalled over 93,000 cases of frozen cooked shrimp on September 23, 2025. The product may contain Cesium-137 due to insanitary manufacturing conditions. Consumers should not consume these products and seek refunds immediately.
Great American Seafood Imports issued a recall for 93,122 cases of frozen raw shrimp skewers on September 23, 2025. The product may contain Cesium-137 due to insanitary manufacturing conditions. Consumers should not consume these skewers and seek a refund.
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.
Sea Port Products Corporation recalled 1,800 cases of Raw Frozen Easy Peel Headless Shell-On White Shrimp. The recall follows concerns about contamination with Cesium-137. Consumers should stop using the product immediately.
RC Outsourcing LLC recalled 2,669 syringes of Bevacizumab on September 22, 2025. The recall stems from a lack of assurance of sterility, raising significant health risks. Healthcare providers and consumers should stop using the product immediately.
Black Sheep Egg Company recalled 23,625 dozen eggs on September 19, 2025, due to potential Salmonella contamination. The affected products include 12-count cartons of Free Range Grade A Large Brown Eggs with UPC 860010568507. Consumers should not consume these eggs and seek refunds.
Black Sheep Egg Company recalled 288,900 dozen Free Range Grade AA Large Brown Eggs on September 19, 2025. The recall follows potential Salmonella contamination. Affected products were distributed in Arkansas, Missouri, Mississippi, Texas, California, and Indiana.
Ascend Laboratories recalled Atorvastatin Calcium Tablets, 80 mg, on September 19, 2025. The recall affects 90-count and 500-count bottles due to failed dissolution specifications. Consumers should stop using the product immediately and consult their healthcare provider.
Black Sheep Egg Company recalled 23,400 dozen Grade AA large white eggs on September 19, 2025, due to potential Salmonella contamination. The recall affects products sold in Arkansas and Missouri, with additional distribution to Mississippi, Texas, California, and Indiana. Consumers should avoid consuming the eggs and seek refunds or replacements.
Alkem Laboratories recalled Atorvastatin Calcium Tablets, 40 mg, on September 19, 2025. The recall affects 90-count, 500-count, and 1000-count bottles due to failed dissolution specifications. Healthcare providers and consumers must stop using the product immediately.
Black Sheep Egg Company recalled 7,200 dozen free range eggs on September 19, 2025. The recall stems from potential Salmonella contamination. Affected products were distributed in Arkansas and Missouri and may have reached several other states.
Black Sheep Egg Company recalled 58,500 dozen brown eggs on September 19, 2025. The recall follows potential Salmonella contamination. The eggs were distributed in Arkansas, Missouri, Mississippi, Texas, California, and Indiana.
Black Sheep Egg Company recalled 16,245 dozen cartons of Free Range Grade A Large Brown Eggs on September 19 due to potential Salmonella contamination. Consumers should not consume the affected product and should seek a refund or replacement. The recall affects eggs sold in Arkansas and Missouri, with additional distribution in Mississippi, Texas, California, and Indiana.
ARVIS recalled 21 units of its Shoulder Surgical Navigation Software on September 19, 2025. A complaint identified issues that may cause implant malalignment and decreased range of motion. Healthcare providers and patients must stop using the software immediately.
Beckman Coulter recalled 571 DxI 9000 Access Immunoassay Analyzers on September 19, 2025, due to a software anomaly. The defect may lead to inaccurate patient test results affecting diagnoses. Healthcare providers must stop using the device immediately and follow recall instructions.
Beckman Coulter recalled 160 DxC 500i Clinical Analyzer modules on September 19, 2025. A software anomaly may cause incorrect manual dilution factors, leading to false patient results. Healthcare providers must stop using the devices immediately to avoid erroneous diagnoses.
Black Sheep Egg Company recalled 20,625 dozen eggs on September 19, 2025, due to potential Salmonella contamination. The eggs were distributed in Arkansas and Missouri and through wholesale locations in several other states. Consumers should not consume these eggs and seek refunds immediately.