Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Minimum severity
Thermos is recalling 8.2 million Stainless King and Sportsman food containers because stoppers can forcefully eject when the container pressurizes, causing impact and laceration injuries to consumers.
Stephan Baby Boo Bunnie toys are recalled because their plastic cube can break into small parts with sharp edges. CPSC received 20 reports of the cube breaking, including one where a child swallowed sharp pieces.
American Honda Motor is recalling about 12,600 model year 2025-2026 CRF250R/RX/RWE and CRF450R/RX/RWE off-road motorcycles due to a defective handlebar clamp that can unexpectedly rotate, posing a crash hazard. One crash has been reported, but no injuries have been reported.
Bayer recalls about 786,100 travel-size Afrin Original nasal spray bottles lacking child-resistant packaging, posing a poisoning risk to young children. Distributed September 2024 through April 2026. No poisonings reported.
Earthtec 7 3/8-inch pool drain covers violate pool safety standards and pose entrapment and drowning hazards. About 211 units sold online via Amazon from October 2025 to April 2026 should be immediately removed and destroyed.
About 2,800 Qumeney Bicycle Light Sets sold on Amazon contain easily accessible button cell batteries that children can ingest, posing risk of serious injury or death. The lights violate mandatory safety standards and lack required warning labels.
DGIVOVO US electric pressure washers lack proper electrical protection and pose a serious risk of electrocution and electrical shock. Consumers should stop using the product immediately and contact the importer for a free replacement or destruction instructions.
Segmart 4-Drawer Dressers sold on Walmart.com are unstable when not wall-anchored, posing tip-over and entrapment hazards to children. About 16,440 units are affected.
Acer is recalling about 510 AES015 folding electric scooters sold in the U.S. because a loose screw can cause the front tube to fold unexpectedly, posing a fall risk.
About 5,190 UHOMEPRO 5-drawer dressers sold at Walmart.com are unstable when not wall-anchored, posing tip-over and entrapment hazards to children. No injuries have been reported.
Build-A-Bear is recalling about 36,000 Heartwarming Hugs Bears because the zipper slider on the side pouch can detach, posing a choking risk to children. One detachment was reported in the UK, with no injuries reported.
Residential Elevators is recalling StrikeLock hoistway door locking devices that can fail and allow the elevator cab to move with the landing door open, creating a risk of falls and serious injury.
Malker Bicycle Light Sets are recalled due to easily accessible button cell batteries that pose an ingestion hazard to children. If swallowed, these batteries can cause serious internal injuries, chemical burns, and death.
About 30,155 1-K Kerosene containers lack required flame mitigation and child-resistant closures, creating risks of flash fire, severe burns, and poisoning. Consumers should stop using immediately and contact Alliance Chemical for a refund.
USDA FSIS issued a public health alert for meat and poultry products containing FDA-regulated dairy ingredients that may be contaminated with Salmonella. No illnesses have been reported to date.
Hepo Adult Portable Bed Rails (model 110039) are recalled for serious entrapment and asphyxiation risks affecting about 2,200 units. No injuries reported. Stop using immediately and contact manufacturer for refund.
Medline Industries has recalled its PICC Tray (Model DYNJ41648A) because the 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded by FDA.
Medline Industries has recalled six medical device kits (arthrogram trays, angiography packs, and neuro packs) because their 510(k) regulatory clearances have been rescinded by the FDA.
Medline Industries is recalling Convenience Kits containing 10mL polycarbonate colored syringes because the products were modified in ways not approved by the FDA. The kits were distributed nationwide and internationally.
Medline Industries is recalling multiple convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects approximately 270,311 units distributed in the US and internationally.
B. Braun Medical Inc. is recalling Dextrose Injection USP 70% in 2000 mL bags nationwide due to lack of assurance of sterility and potential leakage from the diaphragm port after foil removal.
Medline Industries is recalling 12 types of angiography and catheter kits because their 510(k) regulatory clearances have been rescinded. The kits were distributed nationwide.
Medline Industries is recalling multiple Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects products distributed worldwide including the US, Canada, Panama, and Barbados.
LSL Healthcare is recalling IV Start Kits containing Webcol Large Alcohol Prep Pads due to non-sterility concerns. The affected kits were distributed nationwide in Maryland, Illinois, and Minnesota.
Medline Industries is recalling certain Labor Pack kits (Model DYNJ44813D) nationwide because their 510(k) regulatory clearances for Control Syringes, Guidewires, and High-Pressure Tubing have been rescinded.