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
FSIS issued a public health alert for 8-oz Curry Chicken Salad from Mary's Harvest Fresh Foods, shipped to retailers in Oregon and Washington. No illnesses have been confirmed.
Jake's Fireworks recalled about 132,440 World Class Fireworks "Skull Strobe" rockets because they can explode before reaching their intended height. No injuries have been reported.
About 55,350 Fantastic Four drinking cups and Captain America popcorn helmets with LED lights have accessible button cell batteries and lack the warning labels required by Reese's Law.
An additional 195 Cpzzkq baby loungers are recalled because the padding can obstruct an infant's breathing, breaching the mandatory infant support cushion standard. No injuries reported.
Joyin expanded its recall of Sloosh dive sticks to models 40003 and 16154 alongside model 40041. The sticks exceed the federal compression limit and pose an impalement hazard. No injuries reported.
About 1,034 Mommy's Baby Lovely Deluxe Baby Doll Playsets sold on Temu contain small parts that pose a choking hazard to children under three. No injuries reported.
About 91,000 Woodure toddler tower stools can collapse or tip over, with openings a child's torso can pass through. Woodure reports 22 incidents and 15 injuries involving scrapes, cuts and bruises.
105 Mangohood Direct children's tower stools, model LT003, can collapse or tip over, and a child's torso can fit through openings on the front and back. No injuries reported.
Autocar is recalling 2023-2027 ACTT terminal tractors because the ABS Electronic Control Unit may be improperly secured, potentially causing system failure and increasing crash risk.
Medline Industries, LP is recalling specific C-Section convenience kits because they contain Bupivacaine Hydrochloride in Dextrose Injection, USP, which is subject to a voluntary recall due to quality issues.
JB Chemicals and Pharmaceuticals Ltd is recalling 34,020 bottles of Cetirizine Hydrochloride Tablets USP 5 mg because some tablets were found to contain Ranitidine due to cross contamination.
Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 50 mcg, due to subpotency. The recall affects nationwide distribution in the USA and involves specific lot numbers.
Medline Industries, LP is recalling certain MEDLINE medical procedure convenience kits because they contain ICU Medical, Inc. pain management kits that may be ineffective.
Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 150 mcg, lot N02167, due to subpotent drug concerns. The recall affects nationwide distribution in the USA.
Toyota is recalling side curtain air bag assemblies for 2014-2021 Tundra vehicles because improper rolling may cause deployment issues, increasing injury risk.
The FDA is recalling ROHTO OPTIC GLOW sterile eye drops due to a lack of assurance of sterility. The recall affects 1,278,457 cartons distributed nationwide in the U.S.
Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium Tablets, 75 mcg, NDC 0904-6951-61, due to subpotency. The recall affects lots N02172, N02296, and N02288 with expiration dates in July and December 2026, distributed nationwide.
Rohto-Mentholatum (Vietnam) Co., Ltd. is recalling ROHTO Cooling Eye Drops due to a lack of assurance of sterility. The recall affects multiple lots distributed nationwide within the United States.
Total Nutrition Inc is recalling TNVitamins 100% Organic Moringa Capsules and Powder due to Salmonella contamination. The recall affects 8,492 units distributed nationwide.
Medline Industries is recalling 318 medical procedure kits that contain ICU Medical pain management kits with Bupivacaine Hydrochloride in Dextrose Injection due to quality issues that could result in drug ineffectiveness.
Green Jeeva LLC is recalling Organic Moringa Powder (Product code: GJ96) because it may be contaminated with Salmonella.
Medline Industries, LP is recalling specific Medline kits containing B. Braun convenience kits because they include Bupivacaine Hydrochloride in Dextrose Injection, USP, which has been recalled due to quality issues.
Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 25 mcg, due to subpotency. The recall affects nationwide U.S. distribution of specific lot numbers.
Modern Warrior Life, LLC is recalling Modern Warrior Ready dietary supplements because they contain unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
The FDA is recalling 278 Power F2 Powered Fastening Systems made by Ferno-Washington Inc due to potential roller wear and rail deformation that could prevent stretcher movement.