State
73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
FCA US LLC is recalling specific MOPAR steering drag link assemblies for Heavy Duty Ram 2500 and 3500 trucks because a jam nut may loosen, risking loss of steering control.
Tenneco is recalling Clevite-Pullman rear suspension lower control rods installed in Gillig Low Floor buses because the design makes them susceptible to failure over time.
Costway is recalling about 16,000 double baby strollers because they violate federal safety standards, posing fall, entrapment, and strangulation risks to children.
Apotex Inc. is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels.
Triple E is recalling 2020 Wonder W24MB, W24RTB, and W24FTB motorhomes because an improperly tightened electrical connection may short circuit and cause a fire.
GE Healthcare is recalling Giraffe OmniBed infant incubators equipped with Servo Oxygen modules because they may deliver a different oxygen level than displayed.
AvKARE Inc. is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Defibtech is recalling 860 Lifeline PRO AEDs because a component issue may cause the device to abort or fail to deliver a shock.
Forest River is recalling 2020 Palomino Real-Lite campers because window glass may detach from the frame, posing a projectile hazard.
Toyota is recalling 2013-2015 Prius and 2014-2017 Prius V vehicles because excessive voltage in the inverter may cause the hybrid system to shut down, increasing crash risk.
Brake Parts Inc. is recalling aftermarket brake master cylinders for specific Volkswagen models because the piston may pop out, risking a complete loss of braking.
GE Healthcare is recalling Giraffe Incubators with Servo Oxygen modules because they may deliver different oxygen levels than displayed.
Toyota is recalling 2019-2020 RAV4 and 2020 RAV4 Hybrid vehicles because water may enter the steering gear box, causing a loss of electric power steering assist.
Medtronic is recalling 36 units of Bone Void Filler, Small, because the product may not maintain its setting characteristics for the labeled shelf-life, potentially increasing surgical time.
Siemens is recalling MAMMOMAT Revelation mammography systems because a software limitation may make it difficult to remove the vacuum biopsy system if an exam is interrupted.
Vac-Tron is recalling 100 units of 2020 vacuum excavator trailers because they may be missing rear and rear-side reflex reflectors, which reduces visibility and increases crash risk.
Stryker is recalling specific lots of Locking Screws because the blister pack seal may be compromised, meaning sterility cannot be assured.
Resource Optimization & Innovation LLC is recalling Regard SRHS GIC Port A Cath devices because holes in the packaging may compromise the sterile field.
Stryker is recalling specific lots of locking screws because the blister pack seal may be compromised, meaning sterility cannot be assured.
Stryker GmbH is recalling specific End Cap implants because the blister pack seal may be compromised, meaning sterility cannot be assured.
Stryker GmbH is recalling specific Advanced T2 Tibia Compression Screws because the blister pack seal integrity may be compromised, meaning sterility cannot be assured.
Stryker GmbH is recalling specific lots of End Cap T2 Tibia implants because the blister pack seal may be compromised, meaning sterility cannot be assured.
Stryker is recalling specific locking screws because the packaging seal may be compromised, meaning sterility cannot be assured.
Stryker GmbH is recalling specific lots of Locking Screws because the blister pack seal may be compromised, meaning sterility cannot be assured.
Stryker GmbH is recalling specific T2 Humerus End Cap implants because the blister pack seal may be compromised, meaning sterility cannot be assured.