State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Reliance Worldwide is recalling Cash Acme Heatguard TAFR devices because a thermal failure could cause scalding injuries. About 26,000 units are affected.
Bethel Nutritional Consulting is recalling SLIM-K capsules because FDA testing found unapproved ingredients including sibutramine and phenolphthalein.
FDA recalls Shiley tracheostomy tubes due to reports of patient discomfort and breathing difficulties.
Hospira is recalling Bupivacaine Hydrochloride Injection vials because they contain free-floating and embedded iron oxide particles.
Flex-A-Lite is recalling specific electric fan kits because missing fuse holders and insufficient circuit breakers may cause electrical damage and vehicle fires.
Double Insight is recalling Instant Pot Smart pressure cookers because the thermal probe can conduct electricity, posing a shock risk.
Alliance Partners LLC is recalling 21 Nakoma-SL Anterior Cervical Plating System drill guides because screws may advance through the plate during implantation.
Toyota is recalling 108,624 Prius V vehicles because a hybrid inverter component may overheat, potentially causing the vehicle to stop while driving.
Cooper Lighting is recalling about 1.62 million fluorescent fixtures because the sockets can overheat, arc, and melt, posing a fire hazard.
FDA is recalling Shiley Neonatal and Pediatric Tracheostomy Tubes because patients reported discomfort and breathing difficulties after switching to these products.
Teva Pharmaceuticals is recalling Adrucil (fluorouracil injection) vials due to the presence of black particulate matter, including silicone rubber and drug crystals.
New Punjab Sweets Inc. is voluntarily recalling Ladoo snacks because they lack an ingredient label and may contain undeclared nuts, colors, and wheat.
Vermeer is recalling 2012-2015 BC900XL brush chippers because flanges may crack, causing the discharge chute to separate and create a road hazard.
New Punjab Sweets Inc. is voluntarily recalling Rosgula snacks due to undeclared almonds, colors, and wheat.
Maquet is recalling 646 PowerLED, X-TEN, and VOLISTA surgical light systems because suspension arms may grind and release paint chips into the surgical field.
Lifeline Systems is recalling 38 Philips GoSafe Communicator 7000L units because they may fail to sense the phone line under unusual landline conditions.
New Punjab Sweets Inc. is voluntarily recalling Kaju Fry (toasted fried cashews) because the product may contain undeclared cashew nuts.
Bexco is recalling DaVinci brand cribs because a metal bracket can break, creating gaps that pose entrapment, fall, and laceration risks to infants.
New Punjab Sweets Inc. is voluntarily recalling New Punjab Burfi because the Indian snack may contain undeclared almonds, pistachios, and cashews.
New Punjab Sweets Inc. is voluntarily recalling Chum Chum snacks due to undeclared almonds, coconut, wheat, and food colors.
Stradis Healthcare is recalling Neurosurgery Packs because they contain Devon Light Gloves that are subject to a separate recall by Medtronic.
BTE Technologies is recalling 510 Primus rehabilitation devices because the optional Chop / Lift Bar may detach, posing a fall hazard to users.
Olympus is recalling about 1,200 VG 170 digital cameras sold at HHGregg because an improperly installed part poses an electric shock risk. No injuries have been reported.
Stradis Healthcare is recalling Pediatric Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.
Stradis Healthcare is recalling Basic Packs containing Devon Light Gloves because the manufacturer, Medtronic, is recalling the glove component.