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
About 60,250 DR Power walk-behind and tow-behind leaf vacuums are being recalled because pieces can come loose inside the unit or debris can pierce the chute, ejecting material.
About 320 RH 48-inch and 60-inch Natural Antler Chandeliers are being recalled because canopy hardware can break when hung at an angle, causing the fixture to fall.
About 4,155 Vasicar 18-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
Wanli Tire Corporation is recalling Aptany Eco Sendero M/T2 tires because the sidewall may separate, increasing the risk of a crash.
CareFusion 213 is recalling 106,400 units of BD ChloraPrep Triple Swabsticks over a lack of assurance of sterility.
Shenzhen Atomstack Technologies is recalling material processing laser products for lacking a remote interlock connector required under 21 CFR 1040.10(f)(3).
Indian Cookware and Appliance is recalling 10 pieces of Aluminium Hammered Kadai Size 7 over potential contamination due to leachable lead.
Novo Nordisk is recalling Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL prefilled pens, over the presence of particulate matter after hair was found in a prefilled syringe.
Sheathing Technologies is recalling 12 units of Sheathes3D vaginal and rectal ultrasound probe covers because product defects may result in contamination during use, posing an infection risk.
Novo Nordisk is recalling Wegovy (semaglutide) Injection, 1 mg/0.5 mL prefilled pens, over the presence of particulate matter after hair was found in a prefilled syringe.
Tom Bumble is recalling approximately 6,500 units of Nutty Peanut Butter Flake Candy with Peanut & Chocolate over foreign material.
Philips Ultrasound is recalling 1,721 EPIQ Ultrasound Systems used with the X5-1c transducer because the system may experience an unexpected automatic reboot, resulting in damage to the transducer.
Ferndale Laboratories is recalling 24,589 units of Mastisol Liquid Adhesive because the butyrate tube cracks during actuation, rendering the product unusable.
Beaver-Visitec International is recalling 5 BVI Leos Laser and Endoscopy Systems because ferrites specified for the USB cable assembly were not installed as intended.
Glenmark Pharmaceuticals is recalling 96,948 packs of Ondansetron Orally Disintegrating Tablets, 4mg, because the blister packs are not fully sealed and tablets are falling out.
Bendon Publishing is recalling 39,171 units of Paw Patrol and Mickey Mouse heart-shaped gummy candies over an unapproved color additive, chlorophyllin copper complex.
Vortex Surgical is recalling 221 units of its 25ga Illuminated Flex-Tip Laser Probe because some products in the lot are not passing through a 25ga cannula smoothly.
Zydus Pharmaceuticals is recalling 2,136 bottles of traZODONE Hydrochloride Tablets, 100mg, after a product complaint that some tablets had a dent on the plain side of the tablet surface.
Blue Bird is recalling 2026 Vision and All American electric transit buses because wheelchair restraints may fail to lock, increasing injury risk.
Blue Bird is recalling 2022-2024 All American electric transit buses because a loose 12-volt cable may disconnect, causing loss of electrical systems and increasing crash risk.
Rivian is recalling certain 2022-2025 R1S and R1T vehicles that previously had service performed, because the toe link may have been reassembled incorrectly and the joint may separate.
Allwin Powersports is recalling specific LS2 Rebellion helmets that may lack proper impact protection, increasing the risk of injury during a crash.
Volvo Car USA is recalling 40 model year 2025 EX30 vehicles because the high-voltage battery may experience a short circuit and overheat, increasing fire risk.
Mellace Family Brands is recalling 3,024 units of Wegmans Deluxe Mixed Nuts, Unsalted, over potential Salmonella contamination. The FDA has classified the action as Class I.
Wegmans Food Markets is recalling 2,773.9 lbs of grated Locatelli Pecorino Romano cheese because the product may be contaminated with Listeria monocytogenes. The action is Class I.