State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Elkay is recalling water coolers and bottle filling stations because internal screws can break, causing a loose grounding wire and shock hazard.
VTech is recalling Lights & Lullabies travel mobiles because the clamp can break, causing the mobile to fall and potentially injure an infant.
Forest River is recalling 2018 Palomino PaloMini recreational trailers because the propane bottle mounting bracket may break, allowing the bottle to detach and increasing the risk of injury or crash.
VTech is recalling Shake & Sing Elephant Rattles because the ears can break off, posing a choking hazard to young children.
Fieldbrook Foods is recalling ice cream variety packs due to potential Listeria monocytogenes contamination. The products were distributed nationwide, including Puerto Rico.
Fieldbrook Foods is recalling chocolate covered vanilla ice cream bars due to potential Listeria monocytogenes contamination. The products were distributed nationwide, including Puerto Rico.
Fieldbrook Foods is recalling Sundae Shoppe Raspberry Cream Ice Cream Bars due to potential Listeria monocytogenes contamination. The product was distributed nationwide, including Puerto Rico.
Fieldbrook Foods is recalling Orange Cream Ice Cream Bars sold under multiple brand labels due to potential Listeria monocytogenes contamination.
RaySearch Laboratories is recalling RayStation 6 software due to a defect in the proton QA module that may result in incorrect patient dosage calculations.
Merge Healthcare is recalling 1,150 power strips sold with the Merge Hemo System because an input resistor can overheat and cause the unit to smoke.
Pharmedium Services is voluntarily recalling 2,390 syringes of Phenylephrine HCL 100 mcg/mL due to a superpotent drug classification.
Zoll Manufacturing Corp. is recalling 33,670 LifeVest Wearable Defibrillators due to an incorrect service code that may prevent the device from detecting critical defects, potentially leading to defibrillation shock failure.
Roche Diagnostics is recalling 2,517 automated laboratory analyzers due to a software limitation that may cause sample mismatches.
Fuel Helmets is recalling specific models because the securing strap may fail in extreme temperatures, increasing injury risk in a crash.
Ventura Foods is recalling single-serve Italian dressing packets because a plastic foreign object was inadvertently introduced into the product stream.
Ventura Foods is recalling 18 cases of House Recipe Bleu Cheese Dressing & Dip because a plastic foreign object was inadvertently introduced into the product stream.
Owen Mumford USA is recalling Unifine Pentips pen needles because water exposure may have compromised sterility. Consumers should check for discoloration on the protective seal.
Pharmedium Services is recalling 5,002 pre-filled ephedrine sulfate syringes nationwide because the drug was subpotent. The voluntary recall was initiated in October 2017.
Fashion Accessory Bazaar is recalling Pokemon fidget spinner keychains because the center post can fall out, posing a choking hazard. No injuries have been reported.
Hetero Labs is recalling specific lots of Simvastatin 40 mg tablets because a metallic razor blade was found in one bottle.
Phadia US Inc is recalling 70 Phadia 1000 Instruments nationwide because a malfunctioning Retry command may cause solution shortages and affect test results.
Ventura Foods is recalling A&W Papa Sauce because a plastic foreign object was inadvertently introduced into the product stream.
Dainese is recalling 325 AGV Carbon Modular motorcycle helmets because glue may have caused the chin base material to deteriorate, increasing injury risk.
Owen Mumford USA is recalling Unifine Pentips pen needles because water exposure may have compromised sterility. Users should check for discoloration or yellowing of the protective seal.
Unichem Pharmaceuticals is recalling Divalproex Sodium tablets because metronidazole powder was found in one bottle. The product was distributed nationwide.