Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Ascend Laboratories recalls Alkem Atorvastatin Calcium Tablets USP 20 mg for dissolution failures in 2025. Distributed by Ascend Laboratories, Parsippany, NJ, nationwide. The issue: dissolution specifications not met. Stop use immediately and follow recall instructions. Check your NDC numbers to identify affected lots.
Ascend Laboratories recalls Atorvastatin Calcium Tablets USP, 80 mg, in 90-count and 500-count packages nationwide. The recall cites failed dissolution specifications. Health care providers and patients should stop using the recalled tablets and seek guidance from Ascend or their prescribers.
Black Sheep Egg Company recalled 16,245 dozen Free Range Grade A Large Brown Eggs sold at retail locations in Arkansas and Missouri, and through wholesale brokers in Mississippi, Texas, California and Indiana. The cartons carry UPC 860010568538. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refunds or replacements.
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.
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.
Black Sheep Egg Company is recalling 23,400 dozen Free Range Grade AA Medium White Eggs sold at retail and wholesale locations in Arkansas and Missouri. The recall centers on potential Salmonella contamination. Consumers should not consume the eggs and should contact Black Sheep Egg Company for refund or replacement information.
Beckman Coulter recalls 160 DxC 500i Clinical Analyzer Modules and the DxI 9000 Access Immunoassay Analyzer worldwide after a software anomaly could misapply manual dilution factors. The defect affects samples already in progress using the same Sample ID. Stop using the devices immediately and follow the recall instructions. Beckman Coulter will provide instructions via the recall process.
Black Sheep Egg Company recalled 23,400 dozen Free Range Grade AA Large White Eggs sold at retail and wholesale locations in Arkansas and Missouri due to potential Salmonella contamination. Consumers should not eat these eggs. Contact Black Sheep Egg Company, LLC for refund or replacement information.
Black Sheep Egg Company recalls 23,625 dozen free-range Grade A large brown eggs sold in Arkansas and Missouri. The recall is due to potential Salmonella contamination. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refunds or replacements.
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.
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.
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.
EnHomee recalled Fabric 13-Drawer Dressers sold directly by EnHomee Direct due to a tip-over and entrapment hazard. The units do not meet the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and seek a full refund.
Wuensche USA recalls Ambiano Cotton Candy Makers, model 836098, sold at ALDI. The recall cites a fire hazard from the heating element when the sugar receptacle is missing. Consumers should stop using the unit and pursue a refund.
Arizer recalled the Solo II portable vaporizer on 2025-09-18 after reports of overheating lithium-ion batteries. The recall targets units imported by 7111495 Canada. Consumers should stop using the device and pursue a free replacement.
LXDHSTRA recalled baby loungers and crib bumpers on September 18, 2025. The recall covers LXDHSTRA-branded loungers sold online at Amazon. The defect involves suffocation and fall hazards linked to design and ban violations. Stop using immediately and seek a full refund from LXDHSTRA.
Five Below recalls two tabletop fire pits after reports of alcohol fuel flames jetting and spreading. The recall affects devices sold nationwide. Stop using the recalled pits immediately and contact Five Below for a refund. Full refunds available or $5 option; mail-back refunds possible with photo submission.
IcyBreeze recalled the IcyBreeze Buddy portable misting fan due to a charging fire hazard. The recall affects consumers who own the IcyBreeze Buddy with a 1.5-liter water tank and a 10,000 mAh lithium-ion battery. Affected units must be returned for a full refund and disposal guidance. Call 817-900-2664 or visit the recall page to begin the process and receive a $150 credit at Solo Brands brands.
YooxArmor recalled its multi-purpose kids’ helmets sold on Amazon after safety violations. The helmets fail to meet the mandatory bicycle helmet standard for impact attenuation, stability, labeling and certification. Consumers should stop using the helmets and request a full refund from YooxArmor.