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
Medline Industries is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling General Purpose Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling Pediatric IV Kits because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling IV Start Kits because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling suture removal trays because the povidone-iodine prep pads contain less iodine than labeled.
Medline Industries is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than labeled.
A&H Focal Inc. is recalling Power V8 Viagra tablets because they contain sildenafil, an unapproved drug with unestablished safety and efficacy.
Medline Industries is recalling Dressing Change Tray Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.
Keystone RV is recalling 2018 Crossroads Sunset trailers because they may have tires with an incorrect load rating, which could lead to tire failure and a crash.
Claudio Specialty Foods is recalling specific lots of Sapori di Mare Colatura di Alici di Cetura anchovy sauce because the product contains high levels of histamine.
Guymon Extracts Inc. is recalling approximately 4,202 pounds of fully cooked pork products due to a processing deviation that may have allowed pathogen growth.
Olymel S.E.C./L.P. is recalling approximately 4,618 pounds of raw pork products because they were imported from Canada without undergoing required U.S. import re-inspection.
Jaguar is recalling 2018 XE, XF, E-PACE, F-PACE, and F-TYPE vehicles because fuel rail end caps may leak, increasing the risk of a fire.
Whip City Jerky is recalling beef jerky products because they contain milk, a known allergen, that is not declared on the label.
Kawasaki is recalling 2016-2018 Ninja 1000 motorcycles because high impact forces may break transmission gears, increasing the risk of a crash.
Jaguar Land Rover is recalling 2018 Discovery Sport, Range Rover Evoque, and Velar vehicles because fuel rail end caps may leak, increasing the risk of a fire.
BotanicalNow is recalling BodySlim Herbal capsules because FDA analysis found undeclared sibutramine, a substance not approved for use in this product.
Fresh Pak, Inc. is recalling Aunt Mid's brand sliced apples and grapes bags due to potential Listeria monocytogenes contamination. The product was distributed in Michigan, Ohio, and Wisconsin.
Fresh Pak, Inc. is recalling Aunt Mid's Michigan Apples slice bags due to potential Listeria monocytogenes contamination. The product was distributed in Michigan, Ohio, and Wisconsin.
The FDA is recalling Hard Times For Men capsules because they contain undeclared sildenafil and were marketed without an approved NDA or ANDA.
Condies Foods is recalling Fresh Fruit (Item 40781) due to undeclared milk and egg allergens. The product was distributed to Coremark stores in seven western states.
Pharmatech LLC is recalling Leader Liquid Multivitamin Supplement for Infants and Toddlers due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Rugby Liquid Vitamin C Supplement 500 mg due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Rugby D3 Vitamin liquid due to the presence of yeast and potential contamination with B. cepacia.
Fresh Pak, Inc. is recalling 9oz containers of sliced apples potentially contaminated with Listeria monocytogenes.