State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Nissan is recalling specific 2013-2014 models because software may incorrectly classify an occupied passenger seat as empty, potentially deactivating the airbag.
Mack Trucks is recalling certain 2010-2015 models because condensation in the intake manifold may freeze, causing sensor issues that could lead to vehicle fires or burn injuries.
Porsche is recalling 209 model year 2014 911 GT3 vehicles because a piston connecting rod may come loose, potentially causing an engine fire.
Volvo is recalling 2013-2015 VNL and 2013-2014 VNM trucks because condensation in the intake manifold may freeze, causing sensor issues that increase fire risk.
Forest River is recalling 2014 Crusader fifth wheel trailers because a bracket may contact the tire, risking sudden failure and a crash.
Keystone is recalling specific 2013-2014 fifth wheel trailers because the installed Frigidaire microwaves may start on their own, posing a fire risk.
Crossroads RV is recalling 2014 Redwood and Rushmore trailers because the installed microwave may start on its own, potentially causing a fire.
IKEA is recalling children's bed canopies because the mesh fabric poses a strangulation hazard to infants and young children.
Minga Fair Trade Imports is recalling wooden flipping acrobat toys because the paint contains excessive levels of lead, which is prohibited under federal law.
Bedz King is recalling specific bunk bed models with side ladders because a protruding corner post creates an entrapment hazard. No injuries have been reported.
CTV Best Group is recalling BEST Slim weight loss pills because they contain the undeclared drug sibutramine, making them unapproved new drugs.
Biosense Webster is recalling PentaRay Nav and PentaRay Nav ECO catheters because the distal tip may separate from the shaft.
Autocar is recalling 4,192 model year 2008-2014 ACX, WX, and WXLL trucks because condensation in the intake manifold may freeze, potentially causing exhaust flames or vehicle fire.
Autocar is recalling 2010-2014 Xspotter vehicles because condensation in the intake manifold may freeze and interfere with the pressure sensor, potentially causing exhaust flames or fire.
Autocar is recalling 2014 Xpert trucks because condensation in the intake manifold may freeze, causing elevated exhaust temperatures or flames that increase the risk of vehicle fire or burn injury.
Autocar is recalling 2012-2014 Xpert vehicles because seat belt mounting bolts may be insufficiently tight, increasing injury risk in crashes.
Mar Cor Purification is recalling 130 CWP Reverse Osmosis Systems (Models 101, 102, 104, and 106) due to a potential fire hazard from resistive heating in the pump head assembly.
Ganz is recalling three styles of Grumpy Cat plush toys because their eyes can detach, posing a choking hazard to young children.
GE Healthcare is recalling Innova cardiovascular X-ray systems because they may unexpectedly stop delivering X-rays, causing a loss of real-time imaging.
Biomet 3i is recalling 170 Tapered Navigator Certain Surgical Kits because the trays failed to meet required sterility assurance levels during validation testing.
GE Healthcare is recalling Varicam and VG Hawkeye nuclear medicine devices due to a potential safety issue where the detector may drift toward the patient.
Maquet is recalling 1,424 Plegiox Cardioplegia Heat Exchangers because they may fail to reach the desired cardioplegia temperature when used with a heater/cooler unit.
Biomet 3i is recalling 541 Contra-Angle Torque Driver Kits because the trays failed to meet required sterility assurance levels during validation testing.
Smith & Nephew is recalling RENASYS-F XL with Soft Port dressing kits due to inadequate sealing that may prevent fluid evacuation and fail to trigger alarms.
Biomet 3i, LLC is recalling 21 units of the Navigator Surgical Kit because the trays failed to meet required sterility assurance levels during validation testing.