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.
Vanair is recalling 2009-2013 Ford F-350, F-450, and F-550 Super Duty trucks modified with specific air compressor systems because oil leaks may cause a fire.
PACCAR is recalling 2015 Kenworth and Peterbilt trucks because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
Ferrari is recalling 2010-2014 458 models because the front trunk latch may not release, violating safety standards and increasing injury risk.
Lea Industries is recalling about 520 lighted night stands sold in the U.S. and Canada because the under-lighting can overheat and scorch carpets, posing a burn hazard.
L.L. Bean is recalling specific children's sweaters because a spare button can detach and pose a choking hazard. No injuries have been reported.
Jubilant Cadista Pharmaceuticals is recalling Losartan Potassium and Hydrochlorothiazide tablets due to the presence of stainless steel blemishes.
Ford is recalling 2015 Transit cargo vans because windowless sliding doors may lack epoxy reinforcement, increasing the risk of occupant ejection in a side impact crash.
Adrian Steel Company is recalling 28 model year 2012 Ford E-Series vans modified with propane kits. A metal reaction may cause a propane leak, increasing fire risk.
Fagron is recalling six lots of Pentravan Base 2.5 Kg due to the presence of mold. The product is used for prescription compounding.
Zemco Industries is recalling Cavanaugh Smoked Sausage because it contains soy, a known allergen not listed on the label.
Sandoz Incorporated is recalling 1,332 bottles of Alprazolam 0.25mg tablets nationwide because they may contain stainless steel metal particulates.
Ford is recalling 2015 Transit vehicles because brake fluid may leak from rear caliper junctions, potentially increasing stopping distance or causing complete braking loss.
Fagron is recalling six lots of Phytobase Cream, a prescription compounding vehicle, due to the presence of mold.
Chrysler is recalling 2014-2015 Fiat 500L vehicles because the driver's knee airbag may not deploy correctly, increasing injury risk in a crash.
Stryker is recalling InTouch Critical Care Beds because casters may break and fall off, potentially affecting brake functions.
Newmar is recalling 2014 Dutch Star motorhomes because an incorrectly wired headlight harness may cause both headlights and fog lights to fail, increasing crash risk.
Fagron is recalling specific lots of Pentravan Plus Base, a prescription compounding ingredient, because of mold contamination.
Ford is recalling 2015 Lincoln MKC vehicles because visible air bubbles in the windshield may reduce driver visibility and increase crash risk.
Vizio is recalling about 245,000 39- and 42-inch E-Series televisions because the stand assembly can fail, causing the TV to tip over and pose an impact injury risk.
Ra Medical Systems is recalling 435 PHAROS EX-308 Excimer Lasers because they may calibrate with the iris closed.
Teleflex Medical is recalling RUSCH TruLite laryngoscope handles because the handle may heat up and melt the end cap.
Baxter Healthcare is recalling 1,315 FlowCOUPLER implantable devices because some units may lose electrical continuity, preventing proper monitoring of blood flow.
Dermamedics, L.L.C. is recalling Post Procedure Cream because the FDA determined the product is an unapproved new drug and misbranded.
Daiichi Sankyo is recalling specific lots of Benicar HCT tablets because they were not stored at controlled room temperature during shipping.
McKesson Packaging Services is recalling Aspirin DR Enteric Coated Tablets because they failed to meet dissolution specifications at the 12-month time interval.