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
Collins Bus Corporation is recalling 1,429 model year 2012 school and multi-function buses because emergency egress windows may fail to meet federal safety standards.
Collins is recalling 171 model year 2012 school buses because clothing or backpack drawstrings can get caught in the open door, potentially pulling passengers under the vehicle.
Idle Free Systems is recalling certain aftermarket auxiliary power units for heavy trucks due to a potential fire risk from a battery separator defect.
Banner Mountain Sprouts is recalling alfalfa sprouts after USDA sampling found Salmonella. Consumers should discard or return the product.
Henry's Farm Inc. is recalling soybean sprouts due to potential Listeria monocytogenes contamination. The product was distributed in Maryland, Virginia, and Washington, D.C.
Pro Nutech Inc. is recalling 103,280 lbs of Light Dry Roasted Unsalted Split Peanuts because they may be contaminated with Salmonella Typhimurium from a supplier.
Pacific International Marketing is recalling romaine lettuce tied with a rubber band due to a positive field test for Salmonella. The product was distributed in California and Nevada.
Pro Nutech Inc. is recalling Medium Chopped Peanut Granules because they may be contaminated with Salmonella Typhimurium from a supplier implicated in a salmonellosis outbreak.
LEASA Industries is recalling 6 oz containers of Living Alfalfa Sprouts with a Use By Date of 07/02/2012 after a sample tested positive for Salmonella.
Dole Fresh Vegetables Inc is recalling specific lots of Dole brand Hearts of Romaine because an FDA sample tested positive for Listeria monocytogenes.
Dole Fresh Vegetables Inc is recalling Kroger Fresh Selections Greener Supreme salad due to a positive Listeria monocytogenes sample.
Banner Mountain Sprouts Inc is recalling Alfalfa Broccoli Sprouts after USDA sampling found Salmonella. Consumers should discard the product.
Zimmer, Inc. is recalling Pathfinder NXT Fixed Percutaneous Rod Holders because the tip may crack or break during surgery.
Alere San Diego, Inc. is recalling 30,083 Triage BNP kits nationwide due to decreased precision that may cause unpredictable false positive or negative results.
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system is miscalibrated or defective, potentially affecting drug delivery.
GlaxoSmithKline is recalling Trizivir tablets because they may contain foreign Lexiva tablets. Patients should stop using the affected lot and contact their healthcare provider.
Banner Mountain Sprouts is recalling organic sprouts after USDA sampling found Salmonella. Consumers should discard the product.
Maquet is recalling 284 FLOW-i Anesthesia Systems because a technical alarm may be generated if the MAN/AUTO switch is not fully engaged.
Advanced Neuromodulation Systems is recalling Eon Mini Neurostimulation devices due to a workmanship issue that can cause loss of communication or recharging, resulting in loss of pain relief.
Kimberly-Clark is recalling specific lots of Kleenex Foam Hand Sanitizer, Alcohol Free, due to contamination with Burkholderia cepacia complex.
Zimmer, Inc. is recalling the Pathfinder NXT Fixed Percutaneous Rod Holder because the tip may crack or break during surgery.
VistaPharm is recalling specific lots of Hydrocodone Bitartrate & Acetaminophen Oral Solution because impurities exceeded specifications during stability testing.
GE OEC Medical Systems recalled 86 InstaTrak 3500 Plus surgical navigation systems due to software-related issues. The recall was initiated in 2006 but recently classified by the FDA due to administrative delays.
Prevost is recalling 293 model year 2011-2013 X3-45 and XLII-45 Entertainer buses because a power cable may rub against sharp edges, potentially causing a short-circuit or fire.
Wanchese Fish Company is recalling IQF oysters from South Korea because they were processed under insanitary conditions or may be contaminated with filth.