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
Remel, Inc is recalling 97 units of Campy CVA Medium 100/PK, lot R01272, due to customer complaints reporting low to no recovery of Campylobacter Jejuni ATCC 33291. The product was distributed nationwide in AZ, CO, IL, NJ, OH, TN, and WA.
Olympus is recalling 207 units of its Resection Sheath, Model A22043T, after receiving complaints that the ceramic tip can break during use. The recall affects all lots distributed nationwide.
Prime Food Processing is recalling Dried Croaker Fish, 8 oz, because the fish is uneviscerated. The FDA has classified this recall as Class I, its most serious category.
Encore Medical, LP is recalling 14 EMPOWR 3D KNEE implants because they contain incorrect labeling. The recall affects US nationwide distribution.
Hitachi is recalling one Proton Beam Therapy System due to a software anomaly in the patient positioning system that may cause positional discrepancy during treatment.
Olympus is recalling all lots of its Inner Sheath 21 Fr. Model A2660T used in urological procedures due to reports of the ceramic tip breaking during use.
Olympus is recalling all lots of its Inner Sheath, Model A2641, used in urological endoscopic procedures, due to complaints that the ceramic tip can break during use.
Medline Industries is recalling dialysis dressing change kits containing Tego Connectors due to potential silicone seal doming or tearing that may block fluid flow during use.
Min Jiang Food Store, trading as Koi Koi Trading, is recalling frozen Fish Ball in 200 g packs because of undeclared wheat and sesame. The FDA has classified this recall as Class I.
Medline is recalling 8,773 NAIL KIT (Model DYKM1528) units because the sterile saline wound wash may not have been manufactured to the required sterility assurance level for sterile products.
Ajinomoto Foods North America is expanding a recall for frozen fried rice, ramen, and shu mai products due to possible glass contamination. No injuries have been reported.
Ford Motor Company is recalling certain 2025 and 2026 F-250 SD and F-350 SD vehicles due to a potential driveshaft failure that could lead to a loss of power.
TheKiddoSpace is recalling its Children's Montessori Egg Puzzle Toys due to a choking hazard. The recalled toys are intended for children under three years of age and the eggs can block a child's airway, posing a risk of choking and death to children.
Trankerloop is recalling approximately 2,380 baby bath seats because they are unstable and can tip over, posing a risk of serious injury or death from drowning.
Grtard is recalling approximately 130 Grtard Magnet Stick Figure Men Toy Sets because they contain loose magnets that pose a serious injury or death risk if swallowed.
Royal Oak Enterprises is recalling approximately 190,560 Flame Saber Lighters because they lack required child-resistant mechanisms, posing a risk of serious injury or death.
Somgem and Yomin brand lighters are being recalled because they lack required child-resistant mechanisms, posing a risk of serious injury or death from fire and burns.
General Motors is recalling 2012-2013 Buick Regal vehicles in 23 states due to improper corrosion protection on rear suspension toe links, which may fracture and cause loss of control.
TheKiddoSpace is recalling approximately 9,400 fingerpainting kits because they contain hazardous substances and regulated phthalates that pose health risks to children.
Dupray USA is recalling Dupray Neat Steam Cleaners because the boiler can rupture, posing a risk of burns or serious injury. Consumers should stop using the device immediately and contact the manufacturer for a free replacement safety cap.
International is recalling certain 2023-2027 IC Bus CESB school buses because the brake lines may have been installed with incorrect hardware, which can damage the lines and cause a leak.
Surreal Brands is recalling Tubby Tots Fizzy Flask Bath Magic bath foam sets because moisture can build up pressure in the container, causing pieces to eject forcefully.
Olympus Corporation of the Americas is recalling 744 Olympus High Flow Insufflation Units (Model UHI-2) because a software algorithm issue may cause overpressure events.
Art Monkey LLC is recalling 8,500 bottles of Why Not Natural Moringa Capsules because they have the potential to be contaminated with Salmonella.
Lotus Mom Corporation is recalling 9 units of a 4-quart Brass Pital Pot over potential contamination with leachable lead.