These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,168 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Shintenchi recalled 30,000 6-drawer dressers on February 5, 2026. The dressers pose a serious tip-over and entrapment risk to children if not anchored to the wall. Consumers should stop using the dressers immediately and seek a refund.
YITA recalled multiple brands of dressers on February 5, 2026, due to a serious tip-over hazard. The dressers can pose risks of injury or death to children if not anchored to the wall. Consumers should stop using the affected models immediately and seek refunds.
This recall involves Dresbe LED Christmas Headbands. The headbands were sold as a two-pack of novelty headbands, one red headband with candy cane attachments and a green headband with a Christmas tree attachment, each containing three button cell batteries to power LED lights. The headbands have "HB-052" and "DRESBE LED Christmas Headband (2pc)" printed on labels located on the package.
This recall involves Furnulem five-drawer dressers. The wooden, white dressers measure about 31.5 inches tall, 15.75 inches long and 50.2 inches wide. They have a top with recessed power outlets, and each drawer has two round pull knobs. Only dressers that did not come with feet extensions are included in this recall. Model "HK-DS-017-CL-5D-1-W" is printed on the packaging.
Organic Zing Birch Essential Oil bottles were recalled on February 5, 2026, due to poison risks for children. The essential oil contains methyl salicylate, which requires child-resistant packaging. The recall affects an undisclosed number of bottles sold online by Linkers.
Fresenius Kabi Compounding recalled 1,057 bags of Acyclovir Sodium Injection on February 5, 2026. The recall stems from a lack of assurance of sterility, posing a high health risk. Healthcare providers should cease use immediately and contact the manufacturer for guidance.
Fresenius Kabi Compounding recalled its vancomycin HCl injection on February 5, 2026, due to a lack of assurance of sterility. This Class II recall affects all lots distributed nationwide. Healthcare providers and consumers must stop using the product immediately.
Fresenius Kabi Compounding recalled 1,578 bags of vancomycin HCl injection on February 5, 2026. The company cited a lack of assurance of sterility as the reason for the recall. Healthcare providers and consumers should stop using the product immediately.
Fresenius Kabi Compounding recalled 1,410 bags of ketamine HCl injection on February 5, 2026. The recall stems from a lack of assurance of sterility, posing a high health risk. Healthcare providers and consumers must stop using this product immediately.
Fresenius Kabi Compounding recalled 10,548 bags of thiamine HCl injection on February 5, 2026. The recall follows a lack of assurance of sterility, posing a high health risk. Affected products include several lots expiring between February and May 2026.
This recall involves Scepter B62 gas and oil fuel containers. The recalled combination fuel containers are red with black caps and yellow spouts on each end. They have dual chambers with a 6-liter gas capacity on one side and 2.5-liter oil capacity on the other. "Scepter" and "Essence Danger" are embossed on the side of the container.
Ford recalled certain 2025 F-250, F-350, and F-450 vehicles on February 3, 2026. The steering column shifter may detach, preventing the driver from shifting into park. This defect increases the risk of vehicle rollaway and crash.
Ford Motor Company recalled 2025 Explorers due to transmission valve body issues. The problem may cause unexpected vehicle movement, increasing crash risk. Owners received notification letters on April 11, 2025.
Mazda North American Operations recalled certain 2024-2025 CX-50 vehicles on February 3, 2026. The recall affects trailer hitches that may have loose bolts. A detached hitch can create a road hazard, increasing crash risk.
Pro Numb Tattoo Numbing Spray was recalled due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers should stop using the spray immediately and contact Pro Numb Tattoo Numbing Spray LLC for guidance.
Pro Numb Tattoo Numbing Spray was recalled on February 2, 2026 due to cGMP deviations. The product, containing 4% lidocaine, is distributed by Pro Numb Tattoo Numbing Spray LLC. Consumers should stop using it immediately and contact the company for further guidance.
Costco recalled 8,073 packages of Kirkland Signature Mini Beignets on January 31, 2026. The products contain undeclared hazelnut, posing a serious risk to those with allergies. The beignets were distributed in multiple states including California and Texas.
AiTuiTui recalled its Pull String Teething Toys on January 29, 2026, due to a choking risk. The toys do not meet mandatory safety standards, posing a potential risk of serious injury or death. Consumers should stop using the teething toys immediately and contact the manufacturer for a refund.
Primark recalled The Nightmare Before Christmas Glow-in-the-Dark Coloring Set due to a poisoning hazard. The crayons contain high levels of strontium and aluminum, posing risks if ingested. The recall affects products sold from October 2024 through July 2025.
Hobby Lobby recalled Giraffe and Llama plush toys on January 29, 2026, due to a choking hazard. The legs of these toys can detach, releasing small beads that pose a risk to young children. Consumers should stop using the toys immediately and return them for a full refund.