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.
Dancing Star LLC is recalling bulk organic carob powder due to potential Salmonella contamination. The product was distributed nationwide to retail stores.
Terumo is recalling specific Cardioplegia Delivery Sets because a defect in the luer connector can compromise the seal and introduce air into the tubing line.
Setra is recalling one 2012 S407 motorcoach because an undersized steering shaft may separate under heavy load, causing loss of steering.
Hino is recalling 2012-2015 XFC vehicles because the hybrid motor output shaft may break, potentially causing the vehicle to stop moving and increasing crash risk.
Innovative Trailer Design is recalling one 2014 V40TAN49 van trailer due to a potential pivot bolt crack that could cause the axle to separate.
Wabash National is recalling 2014-2016 Van Trailers because defective brake actuators may cause dragging or overheating, increasing the risk of fire and crash.
Baxter Healthcare Corp is recalling 94,224 INTRA VIA containers due to particulate matter found inside the fluid path.
Dancing Star LLC is recalling specific lots of Carob Supergreens Chunks of Energy and Rave Bites Carob Supergreens because they may be contaminated with Salmonella.
AMS Health Sciences is recalling Saba Shark Cartilage Complex dietary supplements due to the potential presence of Salmonella.
Baxter Healthcare is recalling 20,448 units of INTRA VIA containers due to particulate matter found inside the fluid path.
Terumo is recalling specific cardiovascular and perfusion procedure kits because a luer connector defect may compromise the seal and introduce air into the table line.
Cynosure, Inc. is recalling 322 Elite XPL handpieces for the Elite MPX Laser System due to a potential risk of electrical shock when the device is adjusted or removed while powered on.
Harley-Davidson is recalling 2014-2015 FLS Softail motorcycles because they may lack front turn signal lamp-outage detection, increasing crash risk.
Terumo is recalling 165 units of a cardioplegia delivery set line because a luer connector defect can compromise the seal and introduce air into the line.
Terumo is recalling 777 Cardioplegia Delivery Sets because a defect in the luer connector can compromise the seal and introduce air into the tubing line.
Terumo is recalling Custom Cardioplegia Delivery Sets because a defect in the luer connector can compromise the seal and introduce air into the tubing line.
Aqua Lung is recalling buoyancy compensators with SureLock II handles that may detach, posing a drowning risk. Consumers should stop using them and return them for free replacement.
Terumo is recalling 24 units of Custom Cardioplegia Delivery Sets because a luer connector defect may compromise the seal and introduce air into the line.
Zimmer Surgical Inc is recalling 828 Universal Modular Electric/Battery Handpieces because a malfunction allows them to start unexpectedly when connected to a power source.
Stryker is recalling SmartLife Large Aseptic Housings because the top section may separate from the bottom due to insufficient welding.
Stryker is recalling SmartLife Small Aseptic Housings because the top section may separate from the bottom due to insufficient welding.
Apotex Inc. is recalling Candesartan Cilexetil Tablets, 4 mg, because out-of-specification results were observed for specific impurities and total impurities.
Beckman Coulter is recalling the Small Form Factor Console PC for the DxC 600i analyzer because it may experience an 'MFC Exception' error during normal operation.
Eyemart Express Ltd is recalling 76 pairs of prescription eyeglass safety lenses because they did not meet specifications. The lenses were distributed nationwide.
Sun Pharma Global Inc. is recalling specific batches of Venlafaxine Hydrochloride Extended-Release Tablets because they failed dissolution specifications and a 12-month stability time point.