Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Medtronic Neuromodulation recalled 7,123 units of the Vanta Clinician Programmer Application on December 3, 2025. The software may not function as intended, potentially delaying surgical procedures. Healthcare providers and patients must stop using the software immediately.
McCain Foods USA Inc recalled 21,256 cases of Ore-Ida Tater Tots on December 3, 2025. The recall follows reports of clear hard plastic fragments found in the product. Consumers should not consume the product and should seek refunds or replacements immediately.
BMW of North America recalls 2025 X3 xDrive30 and X3 M50 xDrive after rear brake hoses may leak, causing a loss of rear brake function and disabling ABS and DSC. Owner notification letters were mailed May 9, 2025. If you own a 2025 X3 xDrive30 or X3 M50 xDrive, check your VIN now. Contact BMW customer service at 800-525-7417 for remedy details.
Lunds & Byerlys recalled 1,296 cookies on December 3, 2025, due to undeclared allergens including peanuts, eggs, and soy. The recall affects 108 cases of Monster Cookies sold in Minnesota. Consumers should not eat the product and seek a refund.
Zimmer, Inc. recalled 11 units of the Affixus Antegrade Femoral Nails on December 2, 2025. Affected implants may have an undersized distal diameter, posing a risk of fatigue fracture. This defect could cause adverse reactions requiring surgical intervention.
Zimmer recalled 23 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized distal diameter, leading to potential fatigue fractures. Health risks include pain, tissue damage, and the need for surgical intervention.
Audi Q3 vehicles are recalled in 2025 for a rearview camera software issue. The camera control unit may fail at startup, causing the rear view to not display. Audi and Volkswagen owners should contact their respective dealers for details and to verify if their vehicle is affected.
Volkswagen recalls 2025 Atlas and Atlas Cross Sport models from Volkswagen dealers. The automatic transmission may have been manufactured incorrectly, causing a sudden loss of drive power. Letters notifying owners were mailed March 12, 2025, and dealers will replace the transmission at no cost.
Zimmer, Inc. recalled 23 units of the Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized distal diameter, risking implant fatigue fracture. This defect can cause severe health issues, including pain and tissue damage requiring surgery.
Affixus recalled 22 units of its antegrade femoral nailing system on December 2, 2025, due to a risk of implant fatigue fracture. The defect may lead to serious health complications including tissue damage and pain. Consumers and healthcare providers must stop using the affected implants immediately.
Zimmer recalled 24 Affixus Antegrade Femoral Nails on December 2, 2025, due to potential implant fatigue fractures. The defective implants could cause severe health risks, including pain, tissue damage, and the need for additional surgery. Healthcare providers and patients must cease use immediately and follow recall protocols.
Zimmer Inc. recalled 24 units of Affixus Antegrade Femoral Nails on December 2, 2025. The recall follows reports of undersized distal diameters that could lead to implant fatigue fractures. This defect poses a high risk of adverse tissue reactions and requires immediate action.
Zimmer issued a recall for 22 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized diameter, risking fatigue fractures. This defect could lead to severe health complications for patients.
Fazt & Loud LLC recalled its Sour Gummy Bear energy drinks on December 2, 2025. The product contains 300 mg of caffeine instead of the labeled 150 mg. Consumers should stop using the product and seek a refund or replacement.
Zimmer recalled 24 Affixus Antegrade Femoral Nails on December 2, 2025, due to a risk of implant fatigue fracture. Affected implants may cause serious health issues, including tissue damage and pain. Healthcare providers must stop using the device immediately and follow recall instructions.
Affixus recalled its Antegrade Femoral Nailing System on December 2, 2025, due to a potential implant fatigue fracture risk. The recall affects 22 units distributed nationwide in 14 states. Patients should stop using the affected devices immediately to avoid serious health risks.
Zimmer Inc. recalled 23 units of the Affixus Antegrade Femoral Nails on December 2, 2025. Affected implants may have an undersized distal diameter, leading to potential health risks. Patients should stop using the devices immediately and contact their healthcare provider.
Zimmer recalled 11 Affixus Antegrade Femoral Nails on December 2, 2025. Affected implants may fracture, leading to serious health risks. Patients should stop using the device immediately and follow manufacturer instructions.
Zimmer, Inc. recalled the Affixus Antegrade Femoral Nail on December 2, 2025, due to a risk of fatigue fractures. The recall affects three units distributed nationwide across several states. Patients should stop using the device immediately and consult healthcare providers for further instructions.
Zimmer, Inc. recalled 23 Affixus Antegrade Femoral Nails on December 2, 2025. These implants may have an undersized distal diameter that could lead to fatigue fractures. Patients should stop using the device immediately and contact their healthcare provider.