State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Fireworks Over America is recalling Space Monkey multi-effect fireworks because the lit firework can tip over and fire shells at bystanders, posing burn, fire, and impact hazards.
Athens Foods is recalling approximately 168 pounds of beef products because they contain undeclared soy, a known allergen. No adverse reactions have been reported.
Nissan is recalling specific 2015 Altima and 2016 Maxima vehicles because front brake caliper mounting bolts may not be properly tightened, which could reduce braking ability.
Collins is recalling 2006-2016 school buses with Ricon wheelchair lifts where pivot holes may allow bearings to move, risking platform failure.
Club Car is recalling about 11,600 Precedent gas golf and transport vehicles because a hose clamp can wear a hole in the fuel tank, posing a fire risk.
T3 Micro is recalling about 8,400 Twirl 360 curling irons because the clamp can detach, posing a burn hazard. Consumers should stop using the product and contact T3 for a free repair.
Dodgen is recalling 2006-2014 Mobility RVs with specific Ricon wheelchair lifts. Pivot holes may allow bearings to move, risking platform failure and injury.
Nova Bus is recalling 2010-2015 LFS and 2013-2015 LFS Artic transit buses because a passenger counter sensor may pinch a passenger's arm in the door.
Fresca Foods is recalling Sea Salt Crunchy Bean Snacks because ranch-flavored product containing undeclared milk was packaged in sea salt bags.
JD & SN Inc. is recalling 5 syringes of Testosterone Propionate Injectable Solution due to a lack of assurance of sterility.
JD & SN Inc. is recalling Estradiol 18 mg pellets because the company cannot assure the sterility of the product. The recall covers all sterile human compounded drugs within their expiry date.
The FDA is recalling 9 vials of Chorionic Gonadotropin Injectable Solution from Moses Lake Professional Pharmacy due to a lack of assurance of sterility.
The FDA is recalling Estradiol pellets from JD & SN Inc. because the manufacturer cannot ensure the sterile compounded drugs are free of contamination.
JD & SN Inc. is recalling 6 syringes of Dexpantenol Injectable Solution because the FDA identified a lack of assurance of sterility.
JD & SN Inc. is recalling TRIMIX injectable solution because the agency could not ensure the product remained sterile. Patients should stop using the medication and contact their healthcare provider.
JD & SN Inc. is recalling 95 vials of Chorionic Gonadotropin because the FDA could not verify the sterility of the compounded drug.
Moses Lake Professional Pharmacy is recalling Estradiol Pellets because the FDA determined there is a lack of assurance of sterility for the compounded drug.
JD & SN Inc. is recalling 298 units of compounded testosterone pellets because the FDA cannot ensure the product is sterile.
The FDA is recalling 36 syringes of Methylcobalamin Injectable Solution because the manufacturer cannot ensure the product is sterile.
JD & SN Inc. is recalling a compounded injectable solution because the FDA could not ensure the product remained sterile. Patients should stop using the medication and contact their healthcare provider.
Moses Lake Professional Pharmacy is recalling 355 testosterone pellets because the FDA cannot assure they are sterile. Patients should stop using the product and consult a healthcare provider.
JD & SN Inc. is recalling 8 syringes of Vitamin D3 Oil Injectable Solution due to a lack of assurance of sterility.
FDA is recalling a compounded injectable solution due to a lack of assurance of sterility. The product is distributed nationwide.
The FDA is recalling Estradiol pellets compounded by Moses Lake Professional Pharmacy because the firm cannot assure the sterility of the product.
Moses Lake Professional Pharmacy is recalling 30 syringes of compounded injectable cyanocobalamin because the product lacks assurance of sterility.