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
SOOWERY is recalling 8-Drawer Fabric Dressers because they are unstable if not anchored to the wall, posing tip-over and entrapment risks to children.
RootStim is recalling three minoxidil hair regrowth products because the bottles lack required child-resistant packaging, posing a poisoning risk to young children.
QZH.DUAO children's pajama sets are being recalled because they violate mandatory safety standards, posing a risk of serious burn injuries.
Mack Trucks is recalling 2024-2026 Medium-Duty Electric vehicles because a software error may display a false hill start assist message, increasing crash risk.
Ventec Life Systems is recalling V+ Pro Emergency ventilators because an internal cable connector may disconnect, causing system reboots and interruption of ventilation therapy.
Greenwich Rx is recalling 4,319 vials of Glutathione Injection due to microbial contamination of sterile products. The affected lots were distributed nationwide.
Ventec Life Systems is recalling V*Home ventilators because an internal cable connector may disconnect, causing system reboots and interruption of therapy.
Beckman Coulter is recalling 336 SW41 rotors for Optima centrifuges due to a non-conforming microstructure that may cause the rotors to break during use.
EAK Distribution LLC is voluntarily recalling 3,600 packets of Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprouts Seed due to a risk of Salmonella contamination.
El Ruisenor De Mexico, Inc. is recalling Fritura Rueda Papa / Potato Wheel Snack because it contains undeclared wheat. The product is sold in 1lb, 5lb, and 33lb clear plastic packages.
Gardeners Basics is recalling Waltham 29 Broccoli Sprouting Seeds due to a Salmonella risk. The product was sold nationwide online.
Greiner Bio-One is recalling specific VACUETTE blood collection tubes due to EDTA contamination that may cause falsely elevated potassium and decreased calcium results.
El Ruisenor De Mexico, Inc. is recalling Horchata Drink Mix because it contains undeclared milk, a major food allergen.
Ventec Life Systems is recalling 325 VOCSN+Pro ventilators because an internal cable connector may disconnect, causing system reboots and interruption of ventilation therapy.
Voila Juice Company is recalling 100% Squeezed Orange Juice because it was not processed to achieve the required 5-log pathogen reduction.
Shenzhen Techdow Pharmaceutical is recalling Heparin Sodium Injection due to a lack of assurance of sterility. The product was distributed nationwide in the USA.
Ventec Life Systems is recalling VCSN+Pro ventilators because an internal cable connector may disconnect, potentially interrupting ventilation therapy.
Pfizer is recalling 15,815 bottles of Levoxyl (levothyroxine sodium) 175 mcg tablets because stability testing confirmed the drug was subpotent.
Boston Scientific is recalling 1,442 Direxion Torqueable Microcatheters worldwide due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Philips is recalling 13,206 Lumify Diagnostic Ultrasound Systems due to software and connection issues that may prevent scanning or disrupt function, potentially delaying diagnosis or treatment.
Par Health USA is recalling 18,991 vials of Argatroban Injection because they contain particulate matter. The affected vials were distributed nationwide.
AVID Medical is recalling 80 Halyard Anterior Hip Packs because a non-sterile component was not properly sterilized.
Ventec Life Systems is recalling 180 ventilator units because an internal cable connector may disconnect, causing system reboots and interruption of ventilation therapy.
Wild West Seed Inc is voluntarily recalling specific lots of broccoli seeds due to a Salmonella risk. The affected seeds were distributed in 11 U.S. states and the United Kingdom.
Foreign Tire Sales, Inc. is recalling specific Otani tires because the tread may separate, which could cause a loss of vehicle control and increase the risk of a crash.