State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Emerson is recalling specific Fisher pressure relief valves used in cargo tank trailers because they may break and eject, posing risks of injury, fire, or road hazards.
Crossroads is recalling 2015 Zinger Z-1 and Cruiser trailers because incorrect weight labels may lead to overloading and tire failure.
Mitsubishi Fuso is recalling 2012-2015 FEC52, FEC72, FEC92, and FGB72 trucks because the automatic transmission fluid oil cooler hose may burst, potentially causing the transmission to fail and increasing crash risk.
Newmar is recalling 2007-2012 motorhomes because an incorrectly rated circuit breaker for the refrigerator water line may increase fire risk.
Ford is recalling 2013-2014 C-Max, Fusion, Escape, and Lincoln MKZ vehicles because a defect in the Restraint Control Module may prevent airbags and seat belt pretensioners from functioning in a crash.
Polaris is recalling 2015 Victory motorcycles because a transmission spring may be installed incorrectly, potentially causing loss of control.
Mercedes-Benz is recalling 2015 C300 and C400 vehicles because a steering component may disengage, potentially causing loss of control.
Altec is recalling 2011-2014 DC1317 wood chippers because fasteners may fail, causing the cutting disc to detach and injure operators.
Forest River is recalling 2006-2014 Glaval buses equipped with certain Ricon wheelchair lifts because the platform side plate may crack, posing a risk of injury.
Collins is recalling 2006-2014 school buses equipped with specific Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.
Ross Stores is recalling about 840 metal bistro chairs because the seat can fail to attach to the frame, posing a fall hazard.
Shivvers is recalling about 1,650 Country Clipper riding lawn mowers in the U.S. and 261 in Canada because the ignition module can overheat and melt, posing a fire hazard.
Bad Boy Buggies is recalling about 4,460 recreational off-road vehicles because brake issues can reduce braking ability, posing a crash hazard.
Nova Products, Inc. is voluntarily recalling Black Ant capsules because FDA analysis found undeclared sildenafil, an active ingredient in erectile dysfunction drugs.
Nova Products, Inc. is voluntarily recalling XZEN GOLD capsules because FDA testing found undeclared sildenafil and tadalafil.
Vibrant Health is recalling Rainbow Vibrance Hi ORAC Superfood because a raw material used in its manufacture was found to contain Salmonella bacteria.
Nature's Universe is recalling ThinoGenics dietary supplements because they contain undeclared sibutramine and were marketed without FDA approval.
Nova Products, Inc. is voluntarily recalling Xzen 1200 capsules because FDA analysis found undeclared sildenafil and tadalafil, active ingredients in erectile dysfunction drugs.
Nova Products, Inc. is voluntarily recalling African Black Ant capsules because FDA testing found undeclared sildenafil, an active ingredient in erectile dysfunction drugs.
Nova Products, Inc. is voluntarily recalling XZEN Platinum capsules because FDA analysis found undeclared sildenafil and tadalafil.
Vibrant Health is recalling Green Vibrance 15 dietary supplements because a raw material used in manufacturing was found to contain Salmonella bacteria.
Baxter Healthcare is recalling specific lots of 0.9% Sodium Chloride Injection USP bags due to the presence of particulate matter, including fibers and plastics.
American Health Packaging is recalling 137,300 Ibuprofen 600 mg tablets because some cartons were mis-labeled as Oxcarbazepine 300 mg.
Bristol-Myers Squibb is recalling Coumadin for Injection vials because metallic-like and cellulose fiber particles were found in retained samples.
Baxter Healthcare is recalling 390,560 bags of 0.9% Sodium Chloride Injection USP due to the presence of particulate matter, including fibers and plastics.