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
Wilton Industries Inc. is voluntarily recalling 1,638 units of Valentine Chip Crunch Sprinkles nationwide due to undeclared milk.
Wilton Industries is recalling Rainbow Chip Crunch Sprinkles nationwide due to undeclared milk, a major food allergen.
Wilton Industries is recalling Holiday Home Assorted Treat Toppings nationwide due to undeclared milk, a major allergen.
New Flyer is recalling certain 2013-2021 electric buses because firmware errors in the inverters may cause the electric drive system to shut down, increasing the risk of a crash.
The FDA is recalling Bravo pH Capsule Delivery Devices because the capsule may fail to attach to the esophagus, leading to aspiration and potential hospitalization.
Medtronic is recalling Bio-Console 560 devices because an electrical component may fail, causing the pump to stop and potentially producing smoke or a burning odor.
CPSC recalls 1.06 million Greenworks and Powerworks pressure washer spray guns because the plastic connector can break, causing impact injuries.
Zydus Pharmaceuticals is recalling 1,638 packs of Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.
Wilton Industries is recalling 8,742 units of Autumn Assorted Treat Toppings Sprinkles nationwide due to undeclared milk.
Goal Zero is recalling about 7,850 EC8 power cables because the connector pins can deform and overheat, posing a fire hazard. Four reports of overheating or fire have been received, with no injuries.
Nuts.com is recalling diced dried figs because they contain undeclared almonds, a major food allergen.
Wilton Industries is recalling 18,740 units of Holiday Mix Sprinkles nationwide due to undeclared milk, a major food allergen.
Zydus Pharmaceuticals is recalling Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.
FDA recalls CF Delivery Dev Caps Bravo x5 capsules because they may fail to attach to the esophagus, leading to aspiration.
Altec is recalling 2017-2018 aerial devices because rotation bearing fasteners may crack and break, potentially causing the pedestal and turntable to separate.
Stargate is recalling 2018-2019 Dump Trailers because steering arm bolts may shear under heavy load, increasing crash risk.
Rong Shing Trading Inc. is recalling approximately 3,365 pounds of Chinese-style hot pot base containing beef tallow imported from China, a country ineligible to export beef to the U.S.
Mercedes-Benz is recalling specific 2017-2018 models because a steering shaft defect could cause loss of control. Dealers will inspect and replace the shaft free of charge.
Nutrin Distribution Co is recalling 40,500 lbs of Roasted Peanut Splits due to possible Salmonella contamination. The product was distributed to one customer in Pennsylvania.
Adam's Secret Extra Strength 1500 is being recalled because FDA analysis found unapproved drugs tadalafil and sildenafil in the product.
The FDA is recalling Adam's Secret Extra Strength 3000 because it contains unapproved drugs tadalafil and sildenafil.
El Abuelito Cheese, Inc. is recalling various brands of Queso Fresco due to potential Listeria monocytogenes contamination. The product was distributed in six states.
El Abuelito Cheese, Inc. is recalling multiple brands of Quesillo due to potential Listeria monocytogenes contamination. The product was distributed in six states.
Biomerieux is recalling 8,786 VITEK 2 systems worldwide due to a software defect that may cause false susceptible results when using HL7 communication.
ICU Medical is recalling 425,628 bottles of 0.9% Sodium Chloride Irrigation due to the presence of particulate matter.