Browse through 1,551 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
El Rojo Wholesale recalled 2,904 units of Wheat Pellets on September 23, 2025. The product lacks an ingredient list and nutritional panel, posing a risk to consumers. The absence of wheat and Yellow No. 6 could cause serious health issues for those with allergies.
Becton Dickinson & Co. recalled 177 units of the BD BACTEC Blood Culture System on September 23, 2025. Unauthorized access to product service credentials poses a high risk to patient data and device integrity. Healthcare providers must stop using the devices immediately and follow recall instructions.
Becton Dickinson recalled 62 units of its BD MAX System on September 23, 2025. Unauthorized access to product service credentials poses a high risk to data confidentiality and system integrity. The recall affects worldwide distribution, including the U.S., and requires immediate action from users.
Arctic Shores recalled 93,122 cases of frozen cooked salad shrimp on September 23, 2025. The product may contain Cesium-137, a radioactive isotope. Consumers should stop using the product immediately and seek refunds.
Biomet recalled 98 units of its ZipTight Acute AC Joint Implant on September 23, 2025. The recall follows reports of a potential missing slotted button assembly in one lot. Patients and healthcare providers must stop using the device immediately.
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.
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 46,800 dozen eggs on September 19, 2025, due to potential Salmonella contamination. The recall affects loose open skid eggs sold in retail and wholesale locations across Arkansas and Missouri, as well as broker locations in Mississippi, Texas, California, and Indiana. Consumers should not consume the affected eggs and seek refunds or replacements.
Ascend Laboratories recalled atorvastatin calcium tablets on September 19, 2025, due to failed dissolution specifications. The recall affects 90-count, 500-count, and 1000-count bottles. Consumers should stop using these medications immediately.
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.
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.
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.
Ascend Laboratories recalled 141,984 bottles of Atorvastatin Calcium Tablets on September 19, 2025. The recall follows a failure to meet dissolution specifications. Consumers should stop using the product immediately and consult healthcare providers.
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.
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.
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 14,220 dozen eggs on September 19, 2025 due to potential Salmonella contamination. The recall affects Medium Brown Eggs sold in Arkansas and Missouri, with distribution in several other states. Consumers should not consume the eggs and are urged to seek refunds.