State
73,588 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 178 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 39 (22%) are Severe.
Which agencies issued them
These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,588 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Daimler Coaches North America is recalling certain 2018-2020 Setra S407 and S417 coaches because the engine compartment flap may detach, increasing crash risk.
Gillig is recalling 2013-2020 Low Floor buses because a steering component may fail, causing a loss of power assist and increasing crash risk.
Airstream is recalling 2020-2021 Atlas and Interstate motorhomes because suspension bolts may be too long, potentially breaking and affecting vehicle handling.
Hyundai is recalling 272,126 vehicles because an over-tightened 12V accessory socket may overheat and cause a fire.
Land Rover is recalling 2013-2016 Range Rover and 2014-2016 Range Rover Sport vehicles because doors may be unlatched despite appearing closed, increasing crash risk.
Jayco recalls 2019-2021 Entegra Qwest and Jayco Melbourne motorhomes because the front fender liner can chafe the brake hose, causing brake fluid loss and extended stopping distances.
Forest River is recalling 2021 No Boundaries travel trailers because a faulty protection device may cause voltage overload and increase the risk of fire.
Polaris is recalling 2018-2020 Phoenix 200 ATVs because a damaged throttle lever stop can cause a crash. No injuries have been reported.
Certain 2017-2021 Freightliner Cascadia tractor trailers are recalled due to chemical corrosion in the brake modulator valve, which can slow brake release and cause brakes to pull to one side during automatic braking, increasing crash risk.
Kia is recalling 2015-2016 Soul EVs because the parking mechanism may be damaged if the driver shifts to Park before the vehicle stops, potentially causing unintended movement.
A Better You! is recalling Belecoo 535-S baby strollers because they violate federal safety standards, posing entrapment, strangulation, and fall risks to children.
Edens Garden is recalling Wintergreen and Birch Essential Oils because the bottles lack child-resistant caps, posing a poisoning risk to young children.
Jayco is recalling 2017 North Point fifth wheel trailers because leaf springs may fail to support loads, risking tire damage and loss of control.
Polaris is recalling approximately 26,730 Ranger and General utility vehicles because a software defect may cause sudden acceleration after a restart, posing a crash risk.
Avalon Furniture is recalling Cottage Town Bedroom Furniture sold at Rooms To Go because the base coat paint contains lead levels exceeding federal standards, posing a poisoning risk.
Amneal Pharmaceuticals is recalling 192 bottles of Metformin Hydrochloride Extended-Release Tablets, 500 mg, due to N-Nitrosodimethylamine (NDMA) impurity levels above acceptable intake limits.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Amneal Pharmaceuticals is recalling specific lots of Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected NDMA impurity above acceptable intake levels.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected NDMA impurity above acceptable intake levels.
BIOTA Biosciences is recalling Sterile Curcumin 50mg/mL vials due to lack of assurance of sterility and the presence of unapproved ingredients.
BIOTA Biosciences is recalling sterile Cannabidiol and Curcumin vials due to lack of sterility assurance and lack of FDA approval.
Forest River is recalling 2016 Amera-Lite Cargo Van trailers because insufficient drawbar steel thickness may cause fractures, leading to loss of control or detachment.