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 1,200 PNW Components Loam Pedal Gen 2 mountain bike pedals are being recalled because the pedal axle can crack, causing the pedal to detach from the crank.
About 13,200 Isla Rae magnetic wireless chargers are being recalled because the chargers can explode while in use, posing fire and burn hazards.
About 280 BabyBond retractable safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor and become entrapped.
About 26,200 Sangohe adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 2,240 Kori Gey water elf toy kits are being recalled because the button cell battery compartment can be easily accessed and opened by children.
About 3,500 Lterfear Multifunction Pounding Games are being recalled because they contain high-powered magnets that can detach, posing an ingestion hazard to children.
About 9,300 Joyful Journeys baby loungers are being recalled because the sides are too low, the foot openings are too wide, and the loungers have no stand.
About 14,250 YOLAAH bed rails, model BR-01, are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 18,700 Julie and Judah pajama and lounge pants and shorts are being recalled because they violate the mandatory flammability standards for children's sleepwear.
About 4,155 Vasicar 18-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 5,000 Agrish adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 320 RH 48-inch and 60-inch Natural Antler Chandeliers are being recalled because canopy hardware can break when hung at an angle, causing the fixture to fall.
About 1,430 NFSVLB baby bath seats are being recalled because they are unstable, can tip over, and have leg openings that allow a child's torso to become entrapped.
About 870 Rattan 6-Drawer Dressers, model YD001, are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 60,250 DR Power walk-behind and tow-behind leaf vacuums are being recalled because pieces can come loose inside the unit or debris can pierce the chute, ejecting material.
Wanli Tire Corporation is recalling Aptany Eco Sendero M/T2 tires because the sidewall may separate, increasing the risk of a crash.
Tom Bumble is recalling approximately 6,500 units of Nutty Peanut Butter Flake Candy with Peanut & Chocolate over foreign material.
Sheathing Technologies is recalling 12 units of Sheathes3D vaginal and rectal ultrasound probe covers because product defects may result in contamination during use, posing an infection risk.
CareFusion 213 is recalling 106,400 units of BD ChloraPrep Triple Swabsticks over a lack of assurance of sterility.
Novo Nordisk is recalling Wegovy (semaglutide) Injection, 1 mg/0.5 mL prefilled pens, over the presence of particulate matter after hair was found in a prefilled syringe.
Novo Nordisk is recalling Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL prefilled pens, over the presence of particulate matter after hair was found in a prefilled syringe.
Glenmark Pharmaceuticals is recalling 96,948 packs of Ondansetron Orally Disintegrating Tablets, 4mg, because the blister packs are not fully sealed and tablets are falling out.
Ferndale Laboratories is recalling 24,589 units of Mastisol Liquid Adhesive because the butyrate tube cracks during actuation, rendering the product unusable.
Beaver-Visitec International is recalling 5 BVI Leos Laser and Endoscopy Systems because ferrites specified for the USB cable assembly were not installed as intended.
Philips Ultrasound is recalling 1,721 EPIQ Ultrasound Systems used with the X5-1c transducer because the system may experience an unexpected automatic reboot, resulting in damage to the transducer.