State
72,940 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 177 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 30 (17%) are Severe.
Which agencies issued them
These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 8,600 Viofairy Hair Growth Serum are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
About 21,170 bottles of Bazic Silicone Glue are being recalled because the methanol-containing glue is not in child-resistant packaging and is incorrectly labeled "Non-Toxic".
About 7,000 Sefudun 5% Minoxidil Hair Growth Serum Kit are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
Autocar is recalling 2023-2026 Xpeditor vehicles because contact with the drive line yoke may damage the Electronic Stability Control unit, increasing crash risk.
Winnebago is recalling 2026 Access travel trailers because the Gross Axle Weight Rating may be missing from the certification label, which could lead to overloading.
Lamborghini is recalling 2024-2025 Revuelto vehicles because a software error may prevent the rearview camera image from displaying, increasing crash risk.
Medline is recalling 22,565 units of the Full Electric Low Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Medline is recalling 35,694 units of the Full Electric Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Medline is recalling 138,412 units of the Full Electric Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Medline is recalling 15,581 units of the Full Electric Low Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
White Castle System is recalling 1,021 cases of White Castle Original Sliders over undeclared milk and soy.
Medline is recalling 13,245 Semi Electric Lightweight Homecare Beds because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Zero Motorcycles is recalling 2024-2025 DS, DSR, DSRP, and DSR/X motorcycles because a twisted front brake hose may leak fluid and reduce braking ability.
Ducati is recalling certain 2025-2026 Streetfighter V4 and Panigale V4 motorcycles because excessive heat may damage the rear brake hose, resulting in a sudden loss of the rear brakes.
Merit Medical Systems is recalling 18,897 units of its Custom Inflation Kit because the inflation device handle may detach from the syringe during a procedure.
Merit Medical Systems is recalling its Custom Procedure Kit because the inflation device handle may detach from the syringe during a procedure.
Merit Medical Systems is recalling 328,000 units of the Allwell Angioplasty Pack because the inflation device handle may detach from the syringe during a procedure.
Merit Medical Systems is recalling 4,163,123 units of the Merit Medical Inflation Device basixCOMPAK because the inflation device handle may detach from the syringe during a procedure.
About 500 Mikario Trading 5-in-1 convertible baby gyms are being recalled because the floor mats can obstruct an infant's breathing.
Merit Medical Systems is recalling 864 units of its Custom Waste Management Kit Vascular Tray because the inflation device handle may detach from the syringe during a procedure.
ICU Medical is recalling 14,684,607 Tego Connectors because the silicone seal may bulge, separate from the body or tear, which can cause fluid leaks, occluded flow or air infused into the body.
GE HealthCare is recalling 364 Omni Legend PET systems because an intermittent issue can produce a streaking artifact in PET clinical scan images.
Baxter Healthcare is recalling 585 SIGMA Spectrum Infusion Pumps because defective grease on the cam and motor gears could lead to over-infusion or a free-flow situation.
Mazor Robotics is recalling 549 Mazor X robotic guidance systems over software errors that can result in incorrect surgical instrument positioning during spinal surgery.
Zydus Pharmaceuticals is recalling 22,896 bottles of Icosapent Ethyl capsules, 1 gram, because oxidation caused by leakage of the capsule contents has left them subpotent.