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
MillerKnoll is recalling about 700 Eames Desk and Storage Units sold between October 2020 and March 2022 because the tan side panels contain lead paint levels exceeding the federal ban, posing a lead poisoning hazard to young children.
Katadyn North America is recalling about 1,100 Optimus Gemini portable 2-burner stoves because the gas regulator seal can tear, causing a gas leak and fire hazard. No injuries have been reported.
Keswick Creamery is recalling Bovre cheese in multiple flavors due to potential Listeria monocytogenes contamination. The product was distributed to farm stores and farmers markets in Washington DC, Maryland, Virginia, and Pennsylvania.
St. James Smokehouse is recalling Scottish Smoked Salmon due to possible Listeria monocytogenes contamination. The recall affects 11,141 four-ounce packs distributed domestically and internationally.
World Variety Produce is recalling Dutch Red Potatoes with Dijon Mustard Sauce because the sauce packet fails to declare the presence of egg, a common allergen. Consumers with egg allergies who consume the product risk allergic reactions.
FDA recalls TANDEM LIFE LivaNova LIFESPARC Controllers due to critical software failures that cause the device to freeze, crash, or stop displaying data. The controllers are used in cardiopulmonary bypass procedures.
Keswick Creamery is recalling Whole Milk Ricotta cheese sold at farm stores and farmers markets in DC, MD, VA, and PA regions due to potential Listeria monocytogenes contamination.
Southeast Processing Ltd is recalling yellow squash sold in multiple forms due to positive detection of Listeria monocytogenes in product samples. The affected product was distributed to Georgia and South Carolina.
Keswick Creamery is recalling Ploughman Cider Wash Tomme aged raw milk cheese (batch 47) due to potential Listeria monocytogenes contamination. The product was distributed to farm stores and farmers markets in Washington DC, MD, VA, and PA.
Keswick Creamery at Carrock Farms LLC is recalling aged raw milk cheese 'Wallaby' due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Mother's Touch Complete Nutrition for New Babies infant formula is being recalled because it does not conform to FDA safety standards for infant formula sold in the United States.
Keswick Creamery is recalling Pasteurized Quark cheese due to potential Listeria monocytogenes contamination. The cheese was distributed to farm stores and farmers markets in DC, Maryland, Virginia, and Pennsylvania.
Keswick Creamery at Carrock Farms LLC is recalling Vulkwin's Folly Scratch 2 aged raw milk cheese due to potential Listeria monocytogenes contamination. All products manufactured by the firm may be affected.
Keswick Creamery recalls Calverley aged raw milk cheese due to potential Listeria monocytogenes contamination affecting products distributed to farm stores and farmers markets in DC, MD, VA, and PA.
Keswick Creamery is recalling Vermeer Cheese due to potential Listeria monocytogenes contamination. Products were distributed to farm stores and farmers markets in Washington DC, Maryland, Virginia, and Pennsylvania.
Keswick Creamery is recalling Havarti cheese due to potential Listeria monocytogenes contamination. All products manufactured by the firm may be affected.
Belfonte Ice Cream's Chocolate to Die For Premium Ice Cream may contain undeclared peanuts. Affected products were sold at Hy-Vee, Cash Saver, Harps, Price Mart, and Heartland in Kansas City, Tulsa, Columbia, and Springfield areas.
Keswick Creamery is recalling aged raw milk feta cheese due to potential Listeria monocytogenes contamination. The product was distributed to farm stores and farmers markets in DC, Maryland, Virginia, and Pennsylvania.
Angiodynamics is recalling 40 VenaCure EVLT procedure kit units with fiber components that fail dimensional specifications. The defect may damage the sheath, necessitating removal from the patient and potential additional surgical intervention.
Olympus Corporation is recalling certain POWERSEAL electrosurgical sealers due to an out-of-specification component that may allow the retention ring to loosen, potentially delaying surgical treatment.
bioMerieux is recalling 480 VIDAS CMV IgM test kits with invalid calibrations distributed across 18 U.S. states. The calibration errors may affect diagnostic test accuracy.
OSSUR Power Knee prosthetics are being recalled because the battery may dislodge from the device. Approximately 190 units are affected across the United States.
Ambra PACS and ProViewer versions 3.22.2.0 and 3.22.3.0 have a software defect where patient information edits may be lost during initial study processing due to a race condition between database systems.
Cook Incorporated is recalling Lunderquist Ring Torque Wire Guides due to a complete breach in the chevron seal of the packaging, which may compromise device sterility. The recall affects multiple lot numbers distributed nationwide and internationally.
QuVa Pharma is recalling oxytocin injections due to incorrect formulation. Bags contain 0.45% sodium chloride instead of the intended 0.9%.