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
KTM, Husqvarna, and GASGAS are recalling about 3,310 closed course competition motorcycles because the connecting rod can break, posing crash and injury hazards. Owners should stop riding and contact an authorized dealer for a free repair.
NUK First Choice 240 mL glass baby bottles sold on Amazon.com from January 2018 to May 2022 contain lead markings that exceed the federal lead content ban. Lead is toxic to young children if ingested.
Textron Specialized Vehicles is recalling about 1,750 Arctic Cat Alterra 600 and Tracker 600 ATVs because a fuse in the electrical system can fail during operation, causing sudden loss of engine power and headlights, which poses a crash hazard.
Ocean Technology Systems is recalling about 500 underwater communication devices (PowerCom and MilCom models) with RBLi-4 lithium battery packs because water can leak into the battery pack and cause the circuit board to short and ignite after diving, posing a fire hazard.
Navistar is recalling 2018–2021 International LoneStar and 2016–2021 LT vehicles due to defective battery cables that may overheat and cause personal injury or engine stall without warning, increasing crash risk.
Winnebago is recalling certain 2022 Voyage travel trailers because the awning's welded seam may separate, causing it to drop and increase injury risk.
Launch Sequence Euphoria Capsules have been recalled because the product contains undeclared tadalafil, an unapproved active ingredient. The capsules were distributed nationwide in the USA and Canada.
The FDA is recalling Artri Ajo King tablets nationwide after finding they contain undeclared diclofenac, a prescription anti-inflammatory drug. Affected bottles (lot LTARTKNGOMG30220, expiring December 2025) were sold on Amazon.
Launch Sequence Aphrodisia Capsules contain undeclared tadalafil, making them an unapproved drug. The recall involves 500 4-count tins distributed nationwide in the USA and Canada.
Launch Sequence Capsules dietary supplement recalled for containing undeclared tadalafil, an FDA-approved pharmaceutical ingredient. The product was marketed without required drug approval.
FDA recalls Ortiga mas Ajo Rey dietary supplement sold nationwide due to undeclared diclofenac. Product marketed as supplement contains pharmaceutical ingredient not listed on label.
Blazos Pie Shoppe is recalling 9-inch peanut butter cream pies possibly contaminated with Salmonella. The affected products with code dates 6/23 and 6/27 were distributed in Michigan.
Amazon is recalling Artri King herbal supplement tablets nationwide due to FDA laboratory findings of undeclared diclofenac, a pharmaceutical medication not listed on the label. The product was marketed without FDA approval.
Blazos Pie Shoppe is recalling peanut butter cream and chocolate peanut butter cream pie and cup products that may be contaminated with Salmonella.
GE Healthcare anesthesia systems may have reversed oxygen and air transducer connections, potentially affecting proper gas delivery. 5,372 devices worldwide are affected.
Blount Fine Foods is recalling Panera Bread at Home Southwest Corn Chowder due to undeclared wheat. The product poses a health risk to consumers with wheat allergies or celiac disease.
Queen Bee Gardens is recalling Honey Caramels The Mint due to undeclared tree nuts. The product may contain pecans, almonds, coconut, macadamia nuts, or walnuts.
Queen Bee Gardens is recalling Honey Caramels Caramel Apple because the product may contain undeclared tree nuts. The recall affects products sold at ten retail locations and online nationwide.
Chuckanut Bay Foods LLC is recalling cheesecake bite products with labels declaring sunflower lecithin when they actually contain soy lecithin. Soy is a major allergen not properly disclosed to consumers.
Randox Cholesterol diagnostic kits fail to meet stated performance specifications. Calibration issues cause quality control results to fall outside acceptable ranges, potentially delaying test results.
Queen Bee Gardens is recalling Dark Mint Classic Truffles for undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Products were distributed to retail locations in CO, NM, WY and nationwide online.
Aesculap is recalling the Modulift VBR 4MM set screwdriver due to tip deformation during surgical engagement with implants. The device is distributed in CA, FL, GA, IL, OH, and MI.
Hobbs Medical Polypectomy Snares (Catalog No. 7202) may accordion at the proximal end, preventing full closure and potentially causing injury. Specific lots distributed to medical facilities in NC, TX, WA, and Canada are affected.
Aesculap Implant Systems LLC is recalling the LEFT CORONAL BENDER (TEK1939) surgical instrument used in spinal procedures because it may deform implants when used with spinal system devices.
A software error in SurgiCount+ System Application may allow duplicate surgical sponges to be counted without the required documentation prompt. This could allow surgical cases to close without proper verification that all sponges were accounted for.