State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling approximately 1.4 million vehicles due to a potential sudden loss of electric power steering assist, which increases the risk of a crash.
Jaguar Land Rover is recalling 5,238 2014 Range Rovers because a software defect may prevent the turn signal indicator from flashing at a double rate to warn of a malfunction.
Mercedes-Benz is recalling 2014 GL350, GL450, GL550, and GL63 vehicles because the second-row seat may not fold low enough for proper child seat anchoring.
Daimler Trucks is recalling 2014 Freightliner and Western Star trucks because seat belt buckles may fail to release, potentially hindering emergency egress.
Vactor is recalling certain 2010-2014 HXX and 2012-2014 Guzzler Guzzcavator trucks because the water heater may come loose due to incorrect fasteners, posing a road hazard.
Tiffany Coach Builders is recalling 2009-2010 Coach, Limo, and Shuttle Buses because voltage spikes may damage electrical components, increasing the risk of a fire.
Lenovo is recalling about 34,500 ThinkPad notebook computer battery packs in the U.S. because they can overheat and pose a fire hazard.
General Motors is recalling 2014 Cadillac ELR vehicles because the electronic stability control system may fail to alert drivers if disabled, increasing crash risk.
Keystone RV Company is recalling 2014 Summerland, Springdale, Bullet, and Cougar models because brittle frame spring hangers may fracture, increasing crash risk.
Ricon is recalling S and K series wheelchair lifts with armored pendant cables that may not clear the lift, posing a fire risk.
Toyota is recalling 2013 Highlanders because the second-row left seat may not lock in place, increasing injury risk in a crash.
Excel Industries is recalling about 3,700 BigDog and Hustler riding mowers because the seat switch may fail to detect when the rider leaves, posing a risk of injury.
Abbott Diabetes Care is recalling FreeStyle Flash Blood Glucose Monitors because they may produce inaccurate low blood glucose readings when used with specific test strips.
Fabscout Entertainment, Inc. is recalling Clalis capsules because FDA analysis found they contain sildenafil, an undeclared active pharmaceutical ingredient.
Baxter Healthcare is voluntarily recalling 0.9% Sodium Chloride Injection IV solutions due to the presence of particulate matter, including fibers and plastic particles.
Fabscout Entertainment is recalling Silver Sword capsules because FDA analysis found they contain sildenafil, an undeclared active pharmaceutical ingredient.
Baxter Healthcare is recalling 7,388 bags of Clinimix 5/15 sulfite-free IV solution because they contain particulate matter, including wood, sodium citrate, and dextrose.
Baxter Healthcare is recalling 14,574 bags of Clinimix E IV solution found to contain particulate matter, including wood, sodium citrate, and dextrose.
Abbott Diabetes Care is recalling FreeStyle Blood Glucose Monitors because they may produce inaccurate blood glucose readings when used with specific test strips.
Baxter Healthcare is recalling 7,068 bags of Clinimix E IV solution because they contain particulate matter, including wood, sodium citrate, and dextrose.
Hospira is recalling 40,360 vials of Marcaine (bupivacaine hydrochloride) injection because some units contain visible metal particles that discolor the solution.
Baxter Healthcare is voluntarily recalling 105,216 containers of 5% Dextrose Injection due to the presence of particulate matter, including fibers and plastic particles.
Biomet 3i is recalling BellaTek Zirconia Dental Abutments because of reports of fractures. The recall covers 10,454 units distributed worldwide.
Teleflex Medical is recalling Rusch Brochopart endobronchial tubes because the cuff may inflate to one side, preventing a proper seal of the right lung.
Mar Cor Purification is recalling 232 Millenium HX Portable Reverse Osmosis Systems due to high inlet water pressure and solenoid valve issues that could delay dialysis treatment.