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.
AvKARE Inc. is recalling specific lots of Voriconazole Tablets, 200 mg, because they failed impurity specifications for a related compound.
Akorn Inc is recalling Halyard 24-Hour Oral Care Kits containing chlorhexidine gluconate oral rinse due to crystallization and subpotent assay results.
KVK-Tech, Inc. is recalling specific lots of Phentermine Hydrochloride capsules because they failed impurity specifications during stability testing.
Akorn Inc is recalling Halyard 24-Hour Oral Care Kits containing chlorhexidine gluconate oral rinse due to crystallization and subpotent assay results.
General Motors is recalling 2017-2018 GMC Acadia, 2018 Chevrolet Equinox, and 2018 GMC Terrain vehicles because the right front intermediate driveshaft may fracture and separate while driving.
Polaris is recalling about 1,600 2017 GENERAL Base and Hunter recreational off-highway vehicles because inconsistent tire pressure information can lead to improperly inflated tires and a crash hazard.
BMW is recalling specific motorcycles because accessory turn signals may be insufficiently visible to other drivers, increasing crash risk.
Iowa Mold Tooling is recalling 2016-2017 Dominator Contractor trucks because a fuse block may contact the hood, creating an electrical short that increases fire risk.
Command Electronics is recalling specific LED ceiling lights installed in Jayco and Highland Ridge recreational vehicles because they may produce excessive heat, increasing the risk of a fire.
Heartland is recalling 2018 Pioneer recreational trailers because the liquid propane hose may not be secured, allowing the tire to rub through it and cause a leak.
Forest River is recalling 2018 Prime Time recreational trailers because the Federal Placard lists an incorrect Gross Axle Weight Rating, which could lead to axle failure.
Forest River is recalling 2018 Dynamax, Forester, Sunseeker, and Coachmen Prism vehicles because B-pillar tire labels list pressures that are too low.
Blue Bird is recalling 2015-2019 Vision and 2016 All American school buses because unpadded seat studs may cause head injuries in rear crashes.
Tiny Idahomes is recalling 2014-2017 RVs and trailers because the Federal Placard may display an incorrect Gross Vehicle Weight Rating (GVWR). Owners will receive corrected labels by mail.
Cook Medical is recalling Zenith Alpha Thoracic Endovascular Grafts due to reports of graft thrombosis and occlusion, including one patient death.
Cantrell Drug Company is recalling 21,080 syringes of Glycopyrrolate Injection Solution due to a lack of sterility assurance.
Cantrell Drug Company is recalling Diltiazem HCl 125 mg in 5% Dextrose single-dose bags because of a lack of sterility assurance. The recall covers 2,761 bags distributed nationwide.
Cantrell Drug Company is recalling 1,718 bags of Norepinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL due to a lack of sterility assurance.
Cantrell Drug Company is recalling 3,039 bags of Norepinephrine Bitartrate 4 mg in 0.9% Sodium Chloride due to a lack of sterility assurance.
Cantrell Drug Company is recalling specific lots of Rocuronium Bromide Injection Solution due to a lack of sterility assurance. The affected syringes were distributed nationwide in the US.
Cantrell Drug Company is recalling specific lots of Glycopyrrolate Injection Solution due to a lack of sterility assurance. The affected syringes were distributed nationwide.
Cantrell Drug Company is recalling Adenosine in 0.9% Sodium Chloride syringes due to a lack of sterility assurance.
Cantrell Drug Company is recalling 8,928 bags of Norepinephrine Bitartrate 8 mg in 0.9% Sodium Chloride 250 mL due to a lack of sterility assurance.
Cantrell Drug Company is recalling 75,840 syringes of Glycopyrrolate Injection Solution nationwide because of a lack of sterility assurance.
Volkswagen is recalling 2006-2016 CC, Passat, and Passat Wagon vehicles because a fuel pump control module defect may cause the engine to stall, increasing crash risk.