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
Pharmacy Plus, Inc. dba Vital Care Compounder is recalling Prostaglandin E1 Injection Solution after FDA inspection found the products were manufactured in a manner that cannot guarantee sterility.
Baxter Healthcare is recalling Allen Standard Starburst spine positioning components due to adhesive that may not cure correctly, potentially compromising mechanical holding force in surgical head positioning devices.
Medline has recalled LINQ TRAY surgical kits with breather pouch seal openings that could compromise sterility. The recall affects 40 kits distributed nationwide; no injuries have been reported.
Medline is recalling 96 sterile surgical kits (REF DYNJ50099C, Lot 22DBL482) distributed nationwide due to complaints of openings in breather pouches that compromise sterility and increase contamination risk.
Vital Care Compounder is recalling Brilliant Blue G Solution due to inability to assure product sterility. The recall involves 86 vials (Lot 60448) distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Power Plus is recalling about 115 Tora portable power charging stations because the lithium-ion battery can catch fire while charging. Two fires have been reported with no injuries.
Empower Brands recalls about 518,500 BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, posing a burn hazard. The company has received 241 reports of hot water expelling, including 32 reports of burn injuries.
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.
Clarks Americas is recalling three styles of women's navy canvas shoes sold from February to October 2022 because prolonged contact with the shoe material can expose wearers to toxic chemicals benzidine and/or dimethoxybenzidine.
Ford is recalling 2021-2022 Bronco vehicles with rearview camera systems because the camera image may remain displayed after the vehicle shifts out of reverse, potentially distracting drivers and increasing crash risk.
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.
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.
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.
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.
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.
FHS Retail is recalling about 1,700 units of FUUL 1.9L Pure Liquid Paraffin Lamp Oil because the packaging is not child-resistant and the label omits mandatory safety information required by federal law. The product can cause fatal chemical pneumonia or lung damage if ingested.
Reckitt is recalling about 67,000 AirWick Fresh New Day aerosol air fresheners in Fresh Linen and Fresh Waters scents due to a missing corrosion inhibitor in one batch that can cause cans to rupture or leak. No injuries have been reported.
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.
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.
Nationwide recall of 8.4% sodium bicarbonate injection vials due to container defects causing vial breakage and glass fragments when pressurized during preparation.
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.
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.
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.
Encore Medical is recalling EMPOWR hip liner implants because boxes may contain knee inserts instead. This packaging error could delay surgeries. Four units affected in six US states.
Merit Medical Systems is recalling CorVocet Biopsy Systems due to manufacturing defects that may cause the needle to eject when triggered outside the body, risking needle stick injuries to users or patients.