State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Family Dollar is recalling about 32,000 ceramic wax warmer sets sold nationwide because they can produce high flames, posing fire and burn risks.
SharkNinja is recalling Ninja BL660 series blenders because the loose blade assembly poses a laceration risk if the pitcher is inverted. Consumers should follow new instructions to prevent injury.
Eldorado is recalling 2006-2015 shuttle buses equipped with specific Ricon wheelchair lifts. The defect may cause the lift platform to fall out of the vehicle, increasing injury risk.
STIHL is recalling about 140,000 gas-powered edgers, trimmers, and pruners because a defective fuel tank vent can leak gasoline, creating a fire risk.
PNY is recalling T10400 portable battery packs because they can overheat and vent flames, posing fire and burn hazards.
Mahindra USA is recalling about 2,000 eMax compact tractors because fuel lines can break or leak, posing a fire hazard. No injuries have been reported.
Newmar is recalling 2014-2016 Canyon Star motorhomes because a water heater valve defect may cause water to overheat, posing a scalding risk to users.
Winnebago is recalling specific 2008-2012 recreational vehicles because wheelchair lift bearings may shift, causing the platform to fall and injure the operator.
Specialty Manufacturing Co. is recalling Transpec school bus stop arms because a reflective decal may peel loose, reducing visibility and increasing crash risk.
Hamilton Medical is recalling 1,128 HAMILTON-G5 ventilators because suctioning maneuvers can unintentionally suppress ventilation and alarms.
Whole Foods Market is recalling Organic Roquefort Papillon cheese due to potential contamination with Listeria monocytogenes.
Bard Peripheral Vascular is recalling 292 units of the FLAIR Endovascular Stent Graft due to potential deployment failures during use.
Kontos Foods Inc. is recalling 3,392 tubs of Kontos Falafel Mix nationwide due to undeclared wheat allergen.
Mako Surgical Corporation is recalling RIO system locking pins and connectors because the pins are damaged during assembly.
Siemens Medical Solutions is recalling e.cam Gamma Camera systems due to a potential radial brake failure that could allow the detector to drift.
Brainlab AG is recalling Patient Data Manager software versions 2.0.0 through 2.1.0 because objects may display incorrectly when users deselect fused reference datasets.
Philips is recalling HeartStart MRx monitor/defibrillators because they may reboot unexpectedly, interrupting or delaying therapy.
Otto Bock is recalling the Triton Smart Ankle and iOS Galileo app due to a software issue that can cause unexpected foot movement, posing a fall risk.
CareFusion is recalling SmartSite Extension Sets because they may disconnect or leak. The recall affects 21,000 units distributed in the US and Canada.
GE Healthcare is recalling Centricity Universal Viewer versions 6.0 and higher because magnified projection X-ray images may display inaccurate distance measurements.
GE Healthcare is recalling Centricity PACS-IW software because it may display inaccurate distance measurements for magnified projection X-ray images.
Philips is recalling 1,553 HeartStart MRx Monitor/Defibrillators because automated tests may degrade capacitors and the low battery indicator may fail.
Valeant Pharmaceuticals is recalling specific bottles of Fenoglide (fenofibrate) 120 mg tablets because they failed 24-month dissolution testing.
Ivoclar A. G. is recalling specific lots of Helioseal F dental sealant because a production defect caused particles to be larger than defined, resulting in difficulties during extrusion.
ELITech Clinical Systems is recalling specific reagents used on Selectra ProS and ProM systems due to potential drug interference. No complaints have been received.