State
73,576 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 73,576 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 Cephalexin for Oral Suspension because current Good Manufacturing Practice deviations may cause active ingredient levels to fall outside specification limits.
Talladium Inc is recalling 39 Luminesse Zirconia Discs because the linear shrinkage value on the label is incorrect and outside the acceptable range.
Hager & Meisinger is recalling 144 units of SINGLES Carbide dental burs because the US dates on the package label do not match the bar code display.
Teva Pharmaceuticals is recalling Cephalexin for Oral Suspension because test results showed the drug was below the required potency specification.
MicroPort Orthopedics is voluntarily recalling PROFEMUR Titanium and Cobalt Chrome modular necks to replace older package inserts with the most recent revision.
Thor Motor Coach is recalling certain 2018-2021 motorhomes because the tire valve stem extension may contact the rim and become damaged, potentially causing tire pressure loss and crash risk.
Mercedes-Benz is recalling 2020 GLB 250 vehicles because the second row seat may not lock properly, increasing injury risk in a crash.
Jaguar is recalling 2010-2011 and 2017 XJ vehicles because software may cause frontal air bags to deploy improperly in a crash.
Isuzu and Chevrolet are recalling 2018-2021 FTR and 6500XD trucks because a broken starter ground cable could cause a fire. Owners should contact dealers for a free repair.
Oshkosh is recalling Bendix Pressure Switches sold as aftermarket parts because plastic threads may strip, causing air leaks that can reduce braking performance or disable brake lights.
Quadratec is recalling specific Q-Performance Stealth Series winches because high temperatures may cause unintended operation, increasing injury risk.
Forest River is recalling 2014-2016 Vengeance trailers because the Federal Placard may list an incorrect water capacity, risking overload.
Nissan is recalling 2019 Titan vehicles with LED headlights because incorrect aiming marks may cause improper headlight alignment, increasing crash risk at night.
Medique is recalling 31 over-the-counter drugs sold on Amazon.com because the packaging is not child-resistant, posing a risk of poisoning to young children.
Genie is recalling 2020 TZ-50 trailers because bolted joints on the tongue structure may loosen and separate, increasing crash risk.
Ford is recalling 2019-2020 Edge, Transit Connect, Escape, and Lincoln models because loose bolts on the start/stop accumulator may cause a transmission fluid leak and potential fire.
Residential Elevators is recalling about 6,300 traction elevators installed between 2014 and 2017 because the cab can rise unexpectedly and stop abruptly, posing an impact hazard.
iSi Automotive Austria GmbH is recalling specific curtain air bags that may fail to inflate during a crash, increasing the risk of injury.
Wabash National is recalling 2019-2021 Van trailers because aerodynamic skirts may detach, increasing crash risk.
Organic Aromas is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Ford is recalling 2020 Explorer vehicles because second row center seat belt buckles may not be properly secured, increasing injury risk in a crash.
Chrysler is recalling 319,610 vehicles because a software error can cause the rearview camera image to remain displayed after shifting out of reverse, increasing crash risk.
AAA Cosmetica is recalling bio aaa Advance Hand Sanitizer because it contains methanol. Consumers should stop using the product.
Mylan Institutional LLC is recalling Amiodarone Hydrochloride Injection due to a labeling error where cartons may contain the wrong medication.
Mylan Institutional LLC is recalling 1,407 cartons of Tranexamic Acid Injection due to a labeling error that may result in the wrong medication being dispensed.