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
Joonsung Trading Inc is recalling Chirashi Sauce in 1/2 gallon jugs because the label fails to declare soy and wheat allergens present in the product.
Joonsung Trading Inc recalls Mio Salad Dressing due to undeclared egg allergen. The label lists Mayo but fails to declare Egg, creating serious risk for egg-allergic consumers.
Joonsung Trading Inc is recalling Spicy Chicken Sauce in 1/2 gallon plastic jugs because the product contains wheat but the label does not declare it. This poses a serious risk to consumers with wheat allergies.
The FDA is recalling approximately 4,449 Sara Plus Active Floor Lift devices due to a fire hazard. The devices may emit smoke or ignite, posing a risk to users and staff.
Hippie Organics French Beans, 1Lb packages (Lot IM313626) are recalled due to potential Listeria monocytogenes contamination. Alpine Fresh, Inc. notified the FDA after a positive test result.
Damascus Bakery LLC is recalling Bantam Bagels Everybody's Favorite Everything Bagels due to undeclared egg allergen. The affected product was distributed to a consignee in Georgia.
Joonsung Trading Inc recalls Champon Soup Base due to undeclared milk and tuna allergens. Affected 32 oz containers were distributed in Oregon and Washington; products dated before April 14, 2022 are recalled.
Sunomono Vinegar in 5-gallon jugs is recalled due to undeclared soy and wheat allergens. Consumers with allergies should avoid this product.
Escape Trailer is recalling 2018-2021 travel trailers because aluminum burner tubes can fracture, causing a gas leak that may lead to fire.
R.H. Sheppard is recalling specific steering gears that may have been assembled incorrectly, posing a risk of fracture and loss of steering control.
Ford is recalling trailer brake controllers for 2021-2022 F-150s that may fail to apply trailer brakes, increasing crash risk.
McNeilus is recalling 2022 Bridgemaster Mixer Trucks because insufficient clearance between the tire and fender hardware could cause the fender to detach, creating a road hazard.
Avanos Medical is modifying labeling for the Cortrak 2 Enteral Access System and discontinuing the Anonymous Account Mode feature. Users must confirm tube placement per institutional protocol.
Atrium Medical is recalling the iCast Covered Stent System because the balloon or catheter hub may separate from the delivery catheter during use, potentially causing blood clots, vessel blockages, or organ damage.
Abbott Vascular recalls 14,544 Dragonfly OpStar Imaging Catheters due to potential separation of the proximal marker. The affected devices were distributed throughout the US and internationally.
Cardinal Health is recalling Humalog KwikPen insulin lispro pens distributed in New Mexico due to exposure to improper temperatures caused by inclement weather.
Atrium Medical is recalling the Advanta V12 Covered Stent System worldwide for potential separation of the balloon or catheter hub during withdrawal, which may cause procedural delays and serious complications including embolism and organ infarction.
Yes! Enoki Mushrooms (Lot 6021053, UPC 825382736947) distributed to CA, FL, TX, and NY are being recalled because Listeria monocytogenes was detected in the product. Consumers should not consume the product and should discard it.
Doux South Specialties LLC has recalled Bakkavor Curry Cauliflower pickles due to positive Listeria monocytogenes test results. The recall affects 145 five-gallon pails distributed to California and North Carolina.
Plastikon Healthcare LLC is recalling 23,300 antacid suspension cups due to microbial contamination. The product was distributed in Indiana for institutional use.
Plastikon Healthcare LLC is recalling Milk of Magnesia USP (2400 mg/30 mL) distributed in Indiana due to microbial contamination in this non-sterile product. The FDA classified this as a Class I recall.
The 2022 Freightliner Cascadia is being recalled because a faulty valve in the air brake system can trap air and impair braking or lock the rear axle while the truck is moving.
Cross Country is recalling 2022 trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle, increasing crash risk.
Braun Ambulances is recalling 2020-2021 models because a defective circuit board can cause vehicle lighting to fail, increasing crash risk.
Navistar is recalling certain 2022-2023 IC BUS school buses. The steering wheel retaining nut may have been tightened incorrectly, allowing the steering wheel to loosen or detach. Owners should not drive their vehicles until repaired.