State
73,598 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 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Roche Diagnostics is recalling 684 units of Elecsys CA 19-9 reagent because non-reproducible elevated results may affect clinical interpretation.
Vyaire Medical is recalling 116 bellavista 1000 ventilators because they may fail to sound high-priority alarms or respond to touch screen input.
Covidien is recalling Force TriVerse Electrosurgical Kits distributed in EMEA due to potential sterile packaging compromise, which may increase infection risk.
Axia Pharmaceutical is recalling Testosterone Cypionate Injection because the product lacks assurance of sterility. The recall covers specific lots distributed in the U.S., Puerto Rico, Barbados, and the Dominican Republic.
Baxter Healthcare is recalling Revaclear 300 Capillary Dialyzers because of the potential presence of particular matter in the header caps of ten lots.
Siemens Healthcare Diagnostics is recalling Atellica IM Humidity Packs because a software error causes the analyzer to incorrectly eject them as expired.
Custom Foods LLC is recalling Sticky Fingers Bakeries Gluten-Free Scones because wheat is listed in the ingredients, posing a risk to individuals with celiac disease or gluten sensitivity.
Siemens Healthcare Diagnostics is recalling Atellica IM Humidity Packs due to a software error that causes the analyzer to incorrectly eject them as expired.
Teva Pharmaceuticals USA is recalling 3,695 bottles of Mesalamine Delayed-Release Tablets because stability testing showed low dissolution results.
Medtronic is recalling McGRATH X3 Disposable Laryngoscope Blades because they may not fit the video laryngoscope handle or fit too tightly, potentially affecting optical performance.
Polymer Technology Systems is recalling PTS Detect Cotinine in vitro diagnostic devices due to a lack of FDA 510(k) clearance.
Advanced Bionics is recalling SoundWave Professional Suite Software 3.2 because the installation process fails when using the supplied USB drive, though current software versions remain functional.
Axia Pharmaceutical is recalling specific lots of Magnesium Chloride Injection because the company cannot assure the product's sterility.
Spartan Fire is recalling 2019-2020 Gladiator and MetroStar emergency vehicles because the park brake line may loosen, causing sudden deceleration and loss of control.
Ford is recalling 2019 Rangers previously repaired under recall 19V-726 because the replacement HVAC blower motor may have an electrical short that increases fire risk.
Micro Bird is recalling 2004-2021 school and transit buses because the emergency door retaining device may fail to keep the door open, increasing injury risk during evacuation.
Volkswagen is recalling 2019 Arteon vehicles because an incorrectly installed electronic brake booster rod may increase braking force or disconnect, raising crash risk.
Arcimoto is recalling 2019-2020 FUV motorcycles because improperly crimped cable lugs may cause loss of drive power or fire.
Triple E Recreational Vehicles is recalling 2020 Wonder travel trailers because unprotected ceiling light wires can chafe and arc, increasing the risk of a fire.
Joyson is recalling certain rear seat belt retractors because the locking mechanism may not properly restrain occupants, increasing injury risk in a crash.
Concession Nation is recalling 2019-2020 QUAT trailers because the tire and loading information sticker may display incorrect cargo weight, potentially leading to overloading.
RH is recalling about 800 Camino floor lamps sold in the U.S. because the foot switch can overheat or catch fire, posing a fire hazard.
Joules USA is recalling specific children's pajamas and robes because they violate federal flammability standards, posing a burn hazard to children.
ECHO and Shindaiwa are recalling about 67,700 backpack blowers and 6,600 replacement straps because parts can be expelled, posing laceration and impact risks.
IKEA is recalling KULLEN 3-drawer chests because unanchored units pose tip-over and entrapment hazards that may result in death or serious injuries to children.