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.
Mobility Specialists is recalling 2007-2008 Ford E-150 vans with wheelchair lifts where latches may fail, risking occupant falls.
Precision Shooting Equipment is recalling TAC Elite, TAC Ordnance, and Enigma crossbows because they can fire an arrow without the trigger being pulled, posing an injury hazard.
Empress Arts is recalling about 1,400 children's pajama sets because they fail to meet federal flammability standards, posing a risk of burn injuries.
Van Hool is recalling 2004, 2006, and 2013 C2045 coaches because a battery equalizer component may conduct electricity when heated, increasing fire risk.
Starcraft is recalling 49 model year 2014 trailers because brittle frame spring hangers may fracture, potentially causing loss of control and increasing crash risk.
Suzuki is recalling 103 model year 2014 DL650A V-Strom motorcycles because a drive chain link may not have been riveted, which could cause the chain to come off and increase crash risk.
Toyota is recalling 2013 Lexus GS 350 vehicles because a brake pedal switch may fail, causing the vehicle to brake without driver input and increasing crash risk.
Tiffin Motorhomes is recalling specific 2008-2011 recreational vehicles because moisture in LED clearance lights may cause a short circuit, increasing the risk of a fire.
Office Depot is recalling Gibson Leather Task Chairs because the seat plate weld can break, posing a fall hazard. About 1.4 million chairs were sold.
Toyota is recalling 2004-2011 Siennas in specific states because the spare tire carrier cable may corrode from road salt, risking the tire falling off and causing a crash.
Great Dane is recalling 2015 Dry Freight Semi-Trailers because a missing weld could cause trailer separation and increase crash risk.
Cordelia Lighting is recalling Commercial Electric two-lamp fluorescent shop lights sold at Home Depot because loose lamp socket connections can cause electrical arcs and fires.
Toyota is recalling 231 model year 2014 Highlanders because the second row right-hand seat may not fully lock into the track, increasing injury risk in a crash.
Lakeshore Learning Materials is recalling Bristle Builders for Toddlers play sets because animal figure bases can detach, posing a choking hazard to young children.
Toyota is recalling 2014 Highlander and Highlander Hybrid vehicles because improper air bag software may fail to properly restrain larger front passengers in a crash.
Pain Free By Nature is recalling REUMOFAN PLUS tablets because they were marketed without FDA approval and contain undeclared diclofenac and methocarbamol.
Flawless Beauty LLC is recalling Saluta (reduced glutathione) Powder for Injection because it was marketed without an approved NDA/ANDA and is labeled for use as an antidote.
Flawless Beauty LLC is recalling Vitamin C Injection ampoules marketed without an approved NDA/ANDA. The product is sold over the counter with labeling indicating disease treatment.
Flawless Beauty LLC is recalling Relumins Advanced Glutathione injectable solution because it was marketed without an approved NDA or ANDA.
Baxter Corporation is recalling ABACUS TPN Calculation Software because it may calculate incorrect electrolyte quantities and display inaccurate data.
Prime Pak Foods is recalling approximately 23,250 pounds of fully cooked breaded chicken products because they contain undeclared eggs, milk, and wheat.
Fresenius Medical Care is recalling Revision K Actuator Test Boards for 2008-Series Hemodialysis Machines because they may fail to detect a disconnected Ultrafiltration Pump.
Flawless Beauty LLC is recalling Tatiomax powder for injection vials because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Flawless Beauty LLC is recalling Sterile Water for Injection ampoules sold over the counter without an approved NDA or ANDA.
Swanson Health Products is recalling specific lots of Full Spectrum Cilantro herbal supplements due to a potential risk of salmonella contamination.