State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
HelloLife is recalling 370 bottles of Thyroveev homeopathic medicine due to microbial contamination. The product was distributed nationwide and internationally.
Spartan Motors is recalling 2018-2019 Metrostar emergency vehicles because improperly heat-treated wheel studs may fail, potentially causing the wheel to detach.
Multiquip is recalling 2018 Water trailers because incorrect axle ratings may cause failure under load, increasing crash risk.
Daimler Trucks North America is recalling 2018-2019 Freightliner 108SD, 114SD, and Business Class M2 vehicles because an incorrectly installed steering shaft may disconnect the steering wheel from the front wheels.
Livin' Lite is recalling 2017-2019 CampLite travel trailers because the drawbar may crack, causing the trailer to separate from the tow vehicle.
Daimler Trucks is recalling 2019 Freightliner and Western Star trucks because exposed tire sidewall steel cords may cause rapid air loss, increasing crash risk.
Navistar is recalling 2018-2019 International HV and MV trucks because trailer brake lights may not illuminate when the truck brakes are used, increasing crash risk.
Intuitive Surgical is recalling 42,274 da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors because cracks may form in the extension tube, potentially causing fragments to fall into patients.
Beaver Visitec is recalling 800 units of Accu-Temp High Temperature Cautery devices due to a potential loss of sterility caused by packaging defects.
Ohio Medical is recalling 1,443 Care-E-Vac 3 portable suction pumps because a battery terminal may contact the pump, causing an electric short and loss of function.
Intuitive Surgical is recalling 23,064 da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors because cracks in the extension tube may cause plastic fragments to fall into patients.
Cardiovascular Systems Inc is recalling 18 Orbital Atherectomy System Saline Infusion Pumps because they may switch to stand-by during use, requiring a reset to continue treatment.
Diagnostica Stago is recalling STA N¿oplastine¿ CI in-vitro diagnostic kits because quality control values fell outside assigned ranges, potentially affecting prothrombin time test results.
Diagnostica Stago is recalling 24,043 kits of STA N¿oplastine¿ CI Plus reagents because quality control values fell outside assigned ranges, potentially affecting prothrombin time test results.
Pfizer is recalling 1,580 vials of Argatroban Injection because stability testing results were out of specification at the 18-month time point.
Par Pharmaceutical is recalling Pramipexole dihydrochloride extended release tablets because they contain a known impurity at levels exceeding specifications.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Cl- Slides because they do not meet maximum allowable interference claims for triglycerides in serum samples.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Cl- Slides because they do not meet maximum allowable interference claims for triglycerides.
Mylan Pharmaceuticals is recalling 656 bottles of Diltiazem HCl Extended-Release Capsules 120 mg because routine stability testing found out-of-specification related compounds.
Mylan Pharmaceuticals is recalling Diltiazem HCl Extended-Release Capsules 120 mg because routine stability testing revealed out-of-specification results for related compounds.
Forest River is recalling specific 2012-2018 buses because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.
Dexter Axle is recalling specific Torsion Trailer Axles because incorrectly oriented brake mounting flanges may cause premature brake failure, increasing crash risk.
Volkswagen Group of America is recalling 2017-2018 Audi R8 Spyder and Coupe vehicles because transmission fluid may leak from the gearbox ventilation hose, creating a fire risk if it contacts hot engine parts.
Heil Environmental is recalling 2014-2016 garbage trucks because hydraulic oil tank brackets may crack, causing oil leaks that increase crash risk.
Trail King is recalling 2016-2018 ACS and AACS trailers because aluminum cross members may crack, potentially causing the suspension to loosen and increasing crash risk.