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.
Volkswagen is recalling 2020 Tiguan LWB vehicles because third row seat belt anchor bolts may not be properly torqued, increasing injury risk in a crash.
RLC Labs Inc. is recalling Nature-Throid tablets nationwide because they were manufactured under conditions found to be subpotent.
Ford is recalling 2019 F-250 and F-350 trucks because a front axle weld may be improper, increasing crash risk. Dealers will inspect and replace axles if needed.
RLC Labs Inc. is recalling Nature-Throid tablets due to Current Good Manufacturing Practice (CGMP) deviations. The products were manufactured under conditions found to be subpotent.
RLC Labs Inc. is recalling WP Thyroid tablets due to Current Good Manufacturing Practice (CGMP) deviations. The products were manufactured under conditions found to be subpotent.
Real Clean Distribuciones SA de CV is recalling LUX EOI Hand Sanitizing Gel because it contained methanol and was below the label claim for ethanol content.
RLC Labs Inc. is recalling WP Thyroid tablets because they were manufactured under conditions associated with subpotent products.
RLC Labs Inc. is recalling Nature Throid 1.25 Grain thyroid medication because FDA analysis found the product to be subpotent.
RLC Labs Inc. is recalling WP Thyroid tablets because they were manufactured under conditions associated with subpotent products.
Inpeco S.A. is recalling Aptio Automation systems with Sysmex Interface Modules because a firmware defect may mis-associate sample IDs, leading to incorrect or delayed clinical chemistry results.
Specialized Bicycle Components is recalling approximately 36,000 Sirrus, Sirrus X, and Sirrus Sport bicycles in the U.S. because the alloy crank arms can disengage, posing fall and injury hazards.
Siemens Healthcare Diagnostics Inc is recalling specific lots of epoc BGEM Test Cards due to sporadically inconsistent low glucose results that could delay diagnosis or cause unnecessary treatment.
Kobalt 40-volt cordless electric pole saws are being recalled because the switch can fail, causing the saw to continue running and posing a laceration risk.
Integra LifeSciences is recalling 74 units of 13 ft handpiece cables used in dermatome sets because the cables melt after sterilization.
Ford is recalling 2020 Expedition vehicles because the seat belt tension sensor may misclassify a child as an adult. This could cause the airbag to deploy in a crash, increasing injury risk.
Airstream is recalling certain 2021 Basecamp 16 trailers because the tire placard displays incorrect tire size and inflation pressure. If tires are inflated per the incorrect label, they could become dangerously underinflated, increasing crash risk.
Inpeco S.A. is recalling FlexLab laboratory automation systems because firmware issues may cause sample ID mis-association, leading to incorrect or delayed test results.
Inpeco S.A. is recalling 8 FlexLab 3.6 Automation systems because firmware issues may cause sample ID mis-association, leading to incorrect or delayed clinical chemistry results.
RLC Labs Inc. is recalling Nature-Throid tablets due to Current Good Manufacturing Practice (CGMP) deviations. The product was manufactured under conditions associated with subpotency.
Kobalt 40-volt cordless chainsaws are recalled because the switch can weld shut, keeping the saw running. No injuries have been reported.
Integra LifeSciences is recalling 13 dermatome sets because the handpiece cable melts after sterilization, posing a risk to patients and staff.
Terumo is recalling three Ultrasonic Air Sensors because a crimped wire was installed backwards, potentially causing false air bubble alarms during extracorporeal procedures.
Novarad Corporation is recalling NovaPACS Diagnostic Viewer software because the cross-localization feature may inaccurately place reference lines on asymmetrical images.
Caravan Global is recalling about 2,700 Sports Armed/Padded Arm Bagged Chairs sold at H-E-B stores in Texas due to a defect that can cause the seat to rip from the frame.
Motor Coach Industries is recalling 2019 D45 CRT LE coaches because seat belt retractors in the last row may not function, increasing injury risk in collisions.