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 the agency’s own highest classification or reported deaths or serious injuries, 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
General Motors is recalling 2021 Cadillac Escalade vehicles. The daytime running lights may not deactivate when headlights are on, which may cause glare and reduce visibility, increasing crash risk.
Bridgestone is recalling specific Firestone and Bridgestone tires that may have sustained cuts during sorting, posing a risk of sudden air loss and vehicle control loss.
BS Interactive is recalling Stashables Finger Skateboard Ramp Sets because the miniature skateboards and scooters contain lead paint levels exceeding federal limits and fail lead content bans, posing a lead poisoning risk to young children.
Myx is recalling approximately 162,000 MYX I, MYX II, and MYX II Plus exercise bicycles because pedals can loosen or detach during use, causing injury. Myx has received 864 reports of pedal loosening or detachment, including 75 injury reports involving bruises and cuts.
Anker Play Products is recalling about 5,000 Bolt Foldable Children's Scooters sold at discount stores from March through May 2022. The paint contains lead levels exceeding the federal ban, creating a lead poisoning hazard for young children.
Micro Bird is recalling 2021-2023 G5, 2022-2023 MB II, and 2022 T-Series school buses because seat-level rub rails may be incorrectly attached, increasing injury risk.
Tangame Busy Houses, wooden activity toy cubes sold on Amazon, contain lead paint on a zipper, lead in a plastic phone cord, and phthalates in a horn bulb, exceeding federal safety bans. No injuries have been reported.
Rad Power Bikes is recalling about 29,300 RadWagon 4 electric cargo bikes because the tires can unexpectedly go flat or separate, risking falls and crashes. The firm has received 137 reports of tire failures and eight injury reports.
Earth Grown Vegan Garlic & Herb Falafel is being recalled due to possible contamination with Shiga toxin-producing E. coli. The recall affects over 190,000 units distributed across multiple US states.
Earth Grown Vegan Traditional Falafel is being recalled due to possible contamination with Shiga toxin-producing E. coli. The FDA Class I recall affects approximately 190,860 units distributed across multiple U.S. states.
Brenner Tank is recalling 2020 TKLQXDC vehicles because the steering arm may fracture, potentially causing a crash.
Cut Fruit Express is recalling Caribou Coffee Snack Fruit and Cheese Plates due to potential Listeria in the Brie cheese. Affected units were distributed in Minnesota with Use By dates from September 30 to October 9, 2022.
Bulk Tank International is recalling 2020 TKLQXSR trailers because the steering arm may fracture, increasing the risk of a crash.
Golden State Medical Supply Inc. is recalling 2,584 bottles of Atenolol 25mg tablets nationwide. Bottles labeled as Atenolol 25mg actually contain Clopidogrel 75mg tablets—a different medication.
Nationwide recall of 8.4% sodium bicarbonate injection vials due to container defects causing vial breakage and glass fragments when pressurized during preparation.
Quality Trailers Ohio is recalling 2022 A, AW, B, and DH trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle.
Exela Pharma Sciences is recalling 2,123,040 vials of Sodium Bicarbonate 8.4% Injection due to container defects causing vial breakage and glass release when pressurized during product preparation.
Medline is recalling 460 Pre-Op CHG Bathing Kits because the CHG solution and blood culture bottles have expiration dates that don't match the kit label. Expired components could compromise effectiveness.
Certain 2022 Audi and Volkswagen vehicles have a defective rearview camera that may go blank or unresponsive, reducing rear visibility. Dealers will replace the camera for free.
Medline Industries is recalling 1,600 blood culture kits (Reorder # DYNDH1592) because component expiration dates don't match the kit label. Affected components include CHG Solution and Bactec bottle plastic.
Siemens is recalling ARTIS pheno x-ray systems with VE10B software due to three potential software issues that may prevent continued treatment on the affected system, potentially requiring use of an alternate system.
Intuitive Surgical's da Vinci X and Xi surgical systems can inadvertently deliver electrical energy to patients under specific instrument and pedal combinations, creating a risk during surgery.
Wright Medical Technology is recalling one Stryker INBONE Tibial Tray due to an oversized tibial tray lock detail that exceeds product specifications and could affect device functionality.
Merit Medical Systems is recalling 2,894 CorVocet Biopsy Systems because misaligned components may cause the needle to eject unexpectedly when triggered outside the body, risking needle stick injuries.
Aurobindo Pharma USA Inc. is recalling Quinapril/Hydrochlorothiazide Tablets 20mg/12.5mg due to N-nitroso-quinapril impurity above acceptable limits from manufacturing deviations. Affected lots QE2021005-A and QE2021010-A were distributed nationwide.