Browse through 1,540 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
HydroJug recalled 14-ounce children's sport tumblers on December 4, 2025, due to a choking hazard. The rivets on the handle can detach, posing a risk to children. The tumblers were sold in five patterns: Cowgirl, Daisy Checkers, Dinosaur, Sport, and Bows.
KTEBO recalled its Writing Tablet Toys on December 4, 2025, due to a risk of serious injury or death from battery ingestion. The toys violate mandatory safety standards because the battery compartment screw can detach. Consumers should stop using the toys immediately and seek a replacement.
Grizzly Industrial recalled all 15" 3HP heavy-duty planers with model number G0815 on December 4, 2025. The planers pose impact and laceration hazards due to a defect that allows the chip breaker to contact the cutterhead blades. Consumers should stop using the planers immediately and contact Grizzly for a free repair kit.
Little Pea Shop recalled crib bumpers on December 4, 2025. The bumpers violate a federal ban and pose a suffocation hazard. Parents should stop using these products immediately.
Ningbo Tianqi Electronic recalled FUFU&GAGA Murphy wall beds on December 4, 2025. The 215-pound frame can fall, posing impact and laceration hazards. Consumers should stop using the beds and seek refunds immediately.
Primark US recalled water balloon pumps on December 4, 2025, due to a risk of injury. The pumps can generate excessive pressure, causing rupture during use. Consumers should stop using the product immediately and seek a refund.
Lil' Turtles recalled 110 cases of Grandma Belle's Tomato Basil Soup on December 4, 2025. The product contains undeclared milk, posing a risk to consumers with milk allergies. Consumers should stop using the soup and contact the manufacturer for a refund.
BMW of North America recalled certain 2025 X3 30 xDrive and X3 M50 xDrive vehicles due to leaking rear brake hoses. This defect may lead to a loss of rear braking function and the failure of the Antilock Brake System and Dynamic Stability Control. Owners will receive notification letters mailed on May 9, 2025.
Bendon, Inc. recalled 39,171 units of various gummy candies on December 3, 2025. The recall stems from the use of an unapproved color additive, chlorophyllin copper complex. Affected products include Paw Patrol, Mickey Mouse, and SpongeBob Squarepants gummies.
Volkswagen Group of America recalled certain 2024-2025 Audi Q3 vehicles on December 2, 2025. A camera control unit software error may prevent the rearview camera image from displaying. This issue increases the risk of a crash due to reduced rear visibility.
Volkswagen Group of America recalled certain 2025 Atlas and Atlas Cross Sport vehicles due to a manufacturing defect. The defect may cause a sudden loss of drive power, increasing crash risk. Notification letters were mailed on March 12, 2025.
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.
Microbiologics recalled LYFO DISK, Catalog Number 0325L, on December 2, 2025, after reports indicated affected units may fail to recover Campylobacter jejuni. This recall affects one unit, with an additional 16 units added on December 22, 2025. The recall impacts products distributed worldwide, including the United States.
Wegmans recalled 3,024 units of Deluxe Mixed Nuts on December 2, 2025. The recall stems from potential Salmonella contamination. Consumers should not consume the product and seek refunds immediately.
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 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 the Affixus Antegrade Femoral Nailing System on December 2, 2025. Affected implants may have an undersized distal diameter that could lead to implant fatigue fractures. Risks include pain, tissue damage, and potential surgical intervention.
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.
Microbiologics recalled 18 units of KWIK-STIK 6-Pack on December 2, 2025. The kits may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni. Patients and healthcare providers should stop using the device immediately.
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.