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.
McLaren is recalling 122 model year 2014-2015 P1 hybrid vehicles because the secondary hood latch may fail to re-engage, potentially allowing the hood to open while driving.
General Motors is recalling 2,633 model year 2016 Chevrolet Traverse, GMC Acadia, and Buick Enclave vehicles because the third-row left lower seat frame may have welds in incorrect locations.
Highland Ridge RV is recalling specific 2015-2016 fifth wheels and travel trailers because they may be missing a caution label regarding the sewer drain valve.
Trail Boss is recalling one 2013 Bloomer Horse Trailer because a water heater valve may cause overheating, posing a scalding risk.
Roush is recalling 2015 Ford Mustang GT Roush Stage 3 vehicles because a brake caliper guide pin may loosen, reducing rear braking ability and increasing crash risk.
Polaris is recalling about 4,700 model year 2015 snowmobiles because the steering pitman arm or drag link can crack, causing a loss of steering and posing a crash hazard.
Polaris is recalling about 2,230 RZR XP Turbo recreational off-highway vehicles because an oil drain line leak can cause a fire.
General Motors is recalling 2016 Chevrolet Silverado and GMC Sierra trucks because a misplaced mounting stud may cause the air bag sensor housing to fracture, potentially preventing air bag deployment in a crash.
Forest River is recalling 2016 model year recreational trailers that were not equipped with carbon monoxide detectors, increasing the risk of injury to occupants.
Dollar Tree is recalling Assured Burn Relief Gel because the packaging is not child-resistant, posing a poisoning risk if swallowed.
Cooper Tire & Rubber Co. is recalling specific Zeon LTZ tires manufactured in September 2015 because tread cracking or chunking may cause loss of tire pressure, increasing crash risk.
Life Science Pharmacy Inc. is recalling E3 Cream compounded in Harriman, NY, due to potential penicillin cross-contamination.
Geritrex Corp is recalling GRx HiCort 25 suppositories because the FDA determined they are unapproved new drugs and misbranded.
Western Drug is recalling two containers of Butor/Nal/Hydro Nasal Suspension because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Toradol 60mg/mL Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling all lots of Jessners Dermal Solution because the product lacks assurance of sterility. The recall covers distribution in eight US states.
Western Drug is recalling Dep-Estradiol 10 mg/mL Injection because the company cannot ensure the product is sterile. The recall covers 9 containers distributed nationwide.
Western Drug is recalling Squaric Acid 4% Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling all lots of Quad Mix Strong Injections because the company cannot ensure the product is sterile. The recall covers distribution in eight US states.
Western Drug is recalling Furosemide 20 mg/mL solution because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Hydroxocobalamin 1mg Injections because the company cannot guarantee the product is sterile.
Western Drug is recalling 16 containers of Triamcin40/Lido5 mg/mL Sus due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Philips Medical Systems is recalling 16 Allura Xper cardio systems because the monitor ceiling suspension system may fall.
Western Drug is recalling Folic Acid Injection due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Western Drug is recalling 9 containers of PZI 40 Insulin (Human) because the product lacks assurance of sterility.