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
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.
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 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 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 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 40 Cubimana treehouse building toy sets are being recalled because button cell batteries in the LED light piece can be easily accessed by children.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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 Blue sliced cheese sold at Whole Foods after WSDA testing identified potential STEC and E. coli O103 contamination. The FDA classified it Class I.
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.
B. Braun Medical is recalling 13,128 extension sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.
Medtronic Sofamor Danek is recalling 275,260 Catalyft PL and PL40 expandable interbody spacers because the cage may lose height or collapse, risking migration or neurological injury.
B. Braun Medical is recalling 6,650 IV administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.
Mindray is recalling 148 Sevoflurane V90 Electronic Vaporizers used with the A9 Anesthesia System over the potential for anesthesia leakage.
B. Braun Medical is recalling 12,200 IV administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.
B. Braun Medical is recalling 98,688 IV administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.