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.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Micro Bird is recalling 2021-2026 G5, T-Series, and MB II school buses because a loose power cable connection may cause the air conditioning control board to overheat and melt, increasing the risk of a fire.
About 210,000 INIU 10,000mAh power banks, model BI-B41, are being recalled after 15 reports of overheating including 11 fires, three minor burn injuries and over $380,000 in property damage.
Micro Bird is recalling 2022-2026 G5 and T-Series transit buses because a loose power cable connection may cause the air conditioning control board to overheat and melt, increasing the risk of a fire.
Ducati is recalling 2025-2026 Panigale V2 and Streetfighter V2 motorcycles because reversed fuses may cause ABS malfunction and wheel lockup.
Nova Bus is recalling certain water pumps because a loose impeller shaft may cause pump failure, increasing crash risk.
About 250 FUFU&GAGA queen size Murphy wall beds are being recalled after two reports of the 215-pound frame falling during assembly, injuring two consumers.
About 3,170 Primark Water Balloon Pumps are being recalled because they can generate excessive pressure and rupture. Two US reports of cuts to hands and fingers have been received.
Motorcar Parts of America is recalling specific brake calipers for 2008-2025 Ford E-450 Super Duty vehicles because the piston bore wall may not meet specifications, causing the caliper to fracture.
About 40 Cubimana treehouse building toy sets are being recalled because button cell batteries in the LED light piece can be easily accessed by children.
About 9,400 CreateOn Crayola-branded pip-Cubes are being recalled because magnets can come loose if the seams separate, posing an ingestion hazard to children.
About 4,120 Casaottima 13-Drawer Dressers are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.
About 2,300 Grizzly Industrial 15-inch 3HP heavy-duty planers, model G0815, are being recalled because the chip breaker can contact the cutterhead blades and eject debris.
About 300 Little Pea Shop padded crib bumpers are being recalled because they can obstruct an infant's breathing and are banned under the Safe Sleep for Babies Act.
About 10,380 KTEBO writing tablet toys are being recalled because the screw securing the button cell battery compartment does not remain attached as the mandatory toy standard requires.
About 17,000 HydroJug 14-ounce children's sport tumblers are being recalled because the rivets on the handle can come loose, causing the handle to detach and posing a choking hazard.
BMW is recalling 2026 X6, X7, X5, and X5 Plug-In Hybrid models. The instrument panel may prevent the passenger-side airbag from deploying properly during a crash.
Fresenius Kabi is recalling 2,199,850 vials of Famotidine Injection USP after out of limit results were obtained for endotoxin testing. The FDA classified it Class I.
MeriCal is recalling 698,064 units of Member's Mark Super Greens Dietary Supplement over potential contamination with Salmonella Richmond. The FDA classified it Class I.
Glycar SA is recalling 30 SJM Pericardial Patches with EnCap Technology because the impacted lot may not meet the required tensile strength specification. The FDA classified it Class I.
WFM Purchasing is recalling 411 lbs of Whatcom Blue sliced cheese sold at Whole Foods after WSDA testing identified potential STEC and E. coli O103 contamination. The FDA classified it Class I.
FRC Inc is recalling 16 units of Face Rock Creamery Vampire Slayer Garlic Cheddar after an FDA environmental sample found Listeria monocytogenes in the packaging area.
Olympus is recalling 7,803 Single Use Ligating Devices because the ligation loop may fail to release or detach, leaving it unintentionally fixed around patient anatomy.
Glycar SA is recalling 18 SJM Pericardial Patches, 5 x 10 cm, because the impacted lot may not meet the required tensile strength specification. The FDA classified it Class I.
WFM Purchasing is recalling 411 lbs of Whatcom Farmhouse sliced cheese sold at Whole Foods after WSDA testing identified potential STEC and E. coli O103 contamination.
Olympus is recalling 7,023 EVIS EXERA III TJF-Q190V duodenovideoscopes after continued reports of positive cultures and infections, and is updating the reprocessing materials.