State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Promise Pharmacy, LLC is recalling 8 vials of Pyridoxine HCl Injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.
Crate and Barrel is recalling Holiday Bear Acrylic Milk Bottles because the included plastic straw can crack or break, posing a laceration hazard.
Porsche is recalling 14,110 vehicles because the instrument cluster may fail to warn drivers when brake pads are worn out, increasing crash risk.
Volkswagen is recalling 2019 Jetta vehicles because an incorrect driver frontal airbag may have been installed during a service visit, potentially increasing injury risk in a crash.
Cincinnati Sub-Zero is recalling 396 Hemotherm CE Dual Reservoir Cooler/Heater units because fuse clips may stretch, causing overheating and device shutdown.
Signature Orthopedics is voluntarily recalling three Genius Knee Cemented CR Femoral Components due to a product mix-up. The devices were distributed in Florida, New York, and Tennessee.
Philips is issuing a software update for 24 Ingenuity TF PET/CT systems to correct multiple issues identified in the previous software version.
Ottobock is recalling 538 PushValve units because some valve inserts have a diameter smaller than the specification. The valve is used for prosthetic fitting of lower limb amputees.
Valeant Pharmaceuticals is recalling 390 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, potentially affecting drug release.
Signature Orthopedics is recalling 10 Genius Knee Cemented Tibial Components due to a product mix-up. The recall covers units distributed in Florida, New York, and Tennessee.
US Compounding Inc is recalling 1,931 syringes of LET Gel 4% because the labels are missing specific lot and expiration dates.
Valeant Pharmaceuticals is recalling 22 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, potentially affecting drug release.
Ottobock is recalling 110 MagValve units used in prosthetic sockets because some valve inserts have a smaller diameter than specified.
Valeant Pharmaceuticals is recalling 206 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, meaning the drug may not release properly.
Ottobock is recalling PushValve upper parts because some installed valve inserts have a diameter smaller than the specification.
Valeant Pharmaceuticals is recalling 1,023 bottles of Cardizem CD (diltiazem hydrochloride) 120 mg capsules because they failed to meet dissolution specifications.
Valeant Pharmaceuticals is recalling 23,884 bottles of Diltiazem HCl CD capsules because they failed dissolution specifications, potentially affecting drug release.
Dr. Reddy's Laboratories is recalling Esomeprazole Magnesium 40mg capsules because they may contain brown pellets.
Akorn Inc. is recalling 30,794 bottles of COSOPT Ophthalmic Solution because the product failed stability specifications for opalescence.
Luminex Corporation is recalling Verigene BC-GP Utility Kits because they were incorrectly labeled with Amplification Tray labels.
Keystone is recalling 2019 Crossroads Redwood recreational trailers because insufficiently tightened pin box mounting bolts could cause the trailer to separate from the tow vehicle.
Academy Sports + Outdoors is recalling Outdoor Gourmet Turkey Keg turkey fryers because the spout can leak oil, posing a fire hazard.
Kia is recalling 2015-2018 Sedona vehicles with manual front passenger seats because a wiring harness may break, potentially allowing the airbag to deploy and injure a child.
Spartan Motors is recalling 2018-2019 Utilimaster Truck Body and Velocity vehicles because backup camera monitors may display reversed images, increasing crash risk.
Keystone is recalling 2019 Bullet Crossfire recreational trailers because the rear-wall spare tire carrier may detach, creating a road hazard.