State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Michelin is recalling specific Pilot Power 3 sport motorcycle tires because they lack required load and pressure information on the sidewall.
WFSP Foods LLC is recalling approximately 18,672 pounds of Land O Frost sausage products because the packaging fails to declare milk, a known allergen.
Halcore Group is recalling 2013-2016 Horton ambulances because a poorly sealed air conditioner wire harness allows water entry, creating a risk of electrical fire.
Midwest Fire is recalling 2016-2017 All-Poly 2500 and 3000 series fire trucks because a transmission component may fail, preventing the vehicle from pumping water.
Tiffin is recalling 2017 Allegro Open Roads because the driver-side wiper arm may break, reducing visibility and increasing crash risk.
Ford is recalling 2013-2015 Taurus, Flex, MKS, and MKT vehicles because a fuel pump component may overheat, causing the engine to stall or preventing the vehicle from starting.
Whirlpool is recalling about 15,200 microwave hood combinations because internal arcing can ignite plastic components, posing a fire hazard.
Mars Retail Group is recalling M&M's-branded jewelry due to high lead levels. Consumers should stop using the items and return them for a refund.
J.D. North America is recalling All Power portable gasoline generators because the fuel tank can leak, posing explosion, fire, and burn hazards.
Bison Coach is recalling 654 model year 2015-2016 horse trailers because a missing inline fuse on the battery cable could cause overheating and fire during an electrical short.
Cree is recalling LED T8 replacement lamps that can overheat and melt, posing a burn hazard. No injuries have been reported.
Seagrave is recalling 28 Marauder II fire trucks because a transmission component may fail, preventing the vehicle from pumping water at fire scenes.
Baxter Healthcare is recalling VASCU-GUARD Peripheral Vascular Patches due to postmarketing reports of intraoperative and postoperative bleeding, including one fatal outcome.
Golden State Medical Supply Inc. is recalling specific lots of Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, due to failed dissolution specifications.
Medtronic is recalling Valleylab Laparoscopic Flat L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 119,770 units distributed worldwide.
Newly Weds Foods Inc is recalling bulk flour bland breader contaminated with E. coli O121. The product was distributed nationwide in 15, 30, and 50 lb bags or boxes.
Medtronic is recalling Valleylab Laparoscopic Wire L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 50,055 units distributed worldwide.
Medtronic is recalling 3,470 Valleylab Laparoscopic Flat L-Hook Electrodes because the package may be compromised, potentially breaching the sterile barrier.
Medtronic is recalling 1,440 Valleylab Laparoscopic Wire J-Hook Electrodes because the packaging may be compromised, potentially breaching the sterile barrier.
Synthes (USA) Products LLC is voluntarily recalling 182 units of Titanium Single Vector Distractor Bodies because the fastener may separate prematurely from the Proximal Foot Plate.
Synthes (USA) Products LLC is voluntarily recalling 90 units of Titanium Single Vector Distractor Bodies because the fastener may separate prematurely from the Proximal Foot Plate.
Hyundai is recalling specific 2016 Sonata vehicles because the driver-side frontal air bag may not adequately protect the driver's neck in a crash.
Medtronic is recalling 19,200 Valleylab Laparoscopic Flexible Argon Electrodes because the packaging may be compromised, potentially breaching the sterile barrier.
Biomet 3i is recalling 1,648,273 dental implants because pouches may not have been sealed during packing, potentially compromising sterility.
Medtronic is recalling Valleylab Laparoscopic Argon Modified Flat l Electrodes due to a potential sterile barrier breach.