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.
Terex is recalling 2006-2014 TLM series aerial devices installed on Ford F550 vehicles due to a potential frame crack that could cause loss of control.
Sunbeam is recalling about 151,600 Holmes ceramic heaters because they can overheat and pose a fire hazard. Consumers should stop using the units and contact Sunbeam for a refund.
Mazda is recalling 2008-2011 Tribute vehicles because a steering sensor may fail, causing the electric power steering assist to disengage.
PACCAR is recalling 2010-2015 Peterbilt trucks because a blown fuse can disable the side air bag without triggering a warning light, increasing injury risk.
Ford is recalling 2010-2014 Taurus vehicles in 21 states and D.C. because corrosion in the license plate lamp assembly may cause a short circuit and fire.
Ford is recalling 2008-2011 Escape and Mercury Mariner vehicles because the steering torque sensor may fail, causing loss of power steering assist.
Fisher & Paykel Healthcare is recalling infant nasal CPAP prongs and starter kits because the prongs may detach from the tubing, interrupting therapy.
Pfizer is recalling specific lots of Effexor XR 150 mg capsules because a foreign Tikosyn capsule was found in a bottle.
Herbal Give Care Llc is recalling Esbelder Fem Mezcla con L-Carnitina because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Herbal Give Care Llc is recalling Esbelin Siloutte Mezcal Herbal because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Tendex is recalling Naturect Capsules because FDA analysis found the product contains undeclared tadalafil, making it an unapproved drug.
Herbal Give Care Llc is recalling Esbelder Man Herbal Blend because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Herbal Give Care Llc is recalling Esbelin Siloutte Te herbal tea because it contains undeclared sibutramine and related compounds, making it an unapproved new drug.
Human Science Foundation is recalling PRO ArthMax tablets because FDA analysis found unapproved prescription drugs in the product.
Ben Venue Laboratories is recalling 5,131 vials of Acetylcysteine Solution, USP, 10% due to the presence of glass particulate matter.
Herbal Give Care is recalling Esbelder Siloutte dietary supplements because they contain undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Lithonia Lighting is recalling Quantum ELM and ELM2 emergency lights because the circuit board can overheat and cause a fire. Consumers should contact the company for a free repair kit.
Teva Pharmaceuticals is recalling QVAR inhalation aerosol canisters because the delivery system and valve are defective.
Maquet Datascope is recalling 11,881 Intra-Aortic Balloon Pump units worldwide due to a potential fan assembly failure that could cause the power supply to overheat and shut down without warning.
Siemens Medical Solutions is recalling 120 550 TxT Treatment Tables because they may lose calibration during treatment, posing a risk of patient mistreatment.
Zydus Pharmaceuticals USA Inc. is recalling 10,200 bottles of Promethazine Hydrochloride 25 mg tablets because atenolol 25 mg tablets were found mixed into the bottles.
Teva Pharmaceuticals is recalling 17,181 bottles of 2 mg Buprenorphine Hydrochloride Sublingual Tablets because stability testing revealed high out-of-specification impurity levels.
Champion Bus is recalling 2014 Defender shuttle buses because transmission software may cause unintended acceleration, increasing crash risk.
Independent Nutrition Center is recalling Red Yeast Rice High Potency Dietary Supplement because it contains excessive levels of lovastatin, an FDA-approved drug.
Tendex is recalling P-Boost Capsules because FDA analysis found the product contains undeclared tadalafil, making it an unapproved drug.