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.
Teva Pharmaceuticals is recalling specific lots of Buprenorphine and Naloxone Sublingual Tablets because they failed impurity specifications.
Valeant Pharmaceuticals is recalling 844 bottles of Obagi-C Rx System C-Therapy Night Cream because the bottles are missing the product insert and outer carton containing safety instructions.
Shionogi Inc. is recalling 455 bottles of PONSTEL capsules because stability testing showed low dissolution results.
Lakota is recalling 2017-2018 trailers because the rear external load ramp may detach, creating a road hazard.
Polaris is recalling 16,800 RZR 170 recreational off-highway vehicles because fuel tank necks can crack or wiring can overheat, posing fire risks.
Ford is recalling 94,605 vehicles because improperly manufactured bolts may fracture, increasing injury risk in a crash.
Quality Foam is recalling approximately 12,200 mattresses that fail to meet the mandatory federal flammability standard, posing a fire hazard.
PACCAR is recalling 2013-2017 Peterbilt and Kenworth trucks with optional spotlights because a short circuit could cause a fire at the cab fuse block.
D & D Foods is recalling approximately 17,847 pounds of Hy-Vee pepperoni pizza products because they contain undeclared soy lecithin, a known allergen.
R & D Products is recalling Outxpro mosquito zapper LED bulbs because the base can separate, posing an electrical shock hazard. No injuries have been reported.
Piaggio is recalling 2018 Liberty 50 iGet 3V scooters because a rear swing arm nut may loosen, potentially causing a loss of control and crash.
iRover is recalling about 2,800 self-balancing scooters because their lithium-ion batteries can overheat, smoke, catch fire, or explode. No injuries or property damage have been reported.
Temsa is recalling 2014-2018 TS45 motorcoaches because a bent air bellow cover may damage tires, increasing crash risk.
Piaggio is recalling 2014-2017 Fly 150 3V scooters because front brake disc mounting screws may loosen, potentially causing the front wheel to lock up and increasing crash risk.
BMW is recalling 2017 C Evolution and C650 GT scooters because front rims may lack required markings, which could lead to incorrect tire installation and handling issues.
ZORJAR is recalling women's silk scarves sold on Amazon.com because they fail to meet federal flammability standards, posing a risk of burn injuries.
Toyota is recalling 2016 Camry and Avalon Hybrid vehicles because the front drive shaft may separate, potentially causing a loss of propulsion or vehicle roll.
Tremcar is recalling rear impact guards on specific trailers because they may not adequately resist force in a crash, increasing the risk of injury.
Mitsubishi is recalling 2007-2013 Outlander vehicles because water leaks can corrode the wiper motor, potentially causing failure and loss of visibility.
Spartan Motors is recalling 2015-2017 Utilimaster Aeromaster vehicles because a missing ground wire may cause intermittent loss of windshield wiper function, increasing crash risk.
Manhattan Toy is recalling Winkel Colorburst activity toys because plastic tubes can break into small pieces, posing a choking hazard to infants.
Smeal is recalling 2016-2017 Aerial Fire Apparatus vehicles because a hydraulic manifold may not be fully seated, causing fluid leaks and potential injury.
Organic Herbal Supply is recalling ZRECT for Women herbal capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling UPROAR male enhancement capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.
Wildway LLC is recalling specific lots of Coconut Cashew Grain-free Granola due to potential contamination with Listeria monocytogenes.