State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mangiacotti is recalling Ginger Lime Hand Sanitizer Spray due to elevated counts of Serratia liquefaciens bacteria.
Med-Mizer is recalling 191 Retractabed Clinical Contour adjustable beds manufactured before June 7, 2008, due to insufficient welding that could cause bed collapse.
General Motors is recalling specific 2014 Chevrolet Silverado, 2014 GMC Sierra, and 2015 Chevrolet Tahoe vehicles because the steering tie rod may not be properly tightened, risking loss of steering.
Med-Mizer is recalling RetractaBed Clinical Contour adjustable beds due to insufficient welding on the foot cross tube, which may cause bed collapse or rollers to detach.
Alere San Diego, Inc. is recalling INRatio2 PT/INR Professional Test Strips because they may report inaccurately low INR results, potentially affecting warfarin therapy monitoring.
General Motors is recalling 2004-2012 Chevrolet, Pontiac, and Saturn vehicles because a wiring issue can disable crash avoidance features like traction control.
Lodal is recalling 2011-2013 Evo garbage trucks because condensation in the intake manifold may freeze, causing sensor issues that increase the risk of vehicle fire or burn injury.
Med-Mizer is recalling 2,980 RetractaBed Clinical Contour adjustable beds due to insufficient welding on the foot cross tube, which may cause bed collapse.
SpineFrontier is recalling S-Lift Lock Shaft Inserters because the impact cap or pin may break during spinal surgery, potentially releasing fragments into the sterile field.
General Motors is recalling specific 2014 Chevrolet Malibus because a software issue may cause a complete loss of brake vacuum assist, increasing stopping distance.
Dimension Industries is recalling Fairview 7-Piece Patio Woven Dining Sets sold at Costco because chair legs can bend and break, posing a fall hazard.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur XP Immunoassay systems because gas springs may fail, causing the instrument cover to fall.
Mangiacotti is recalling Clementine Hand Sanitizer Spray due to elevated counts of Serratia liquefaciens bacteria.
Siemens Healthcare Diagnostics is recalling specific lots of the ADVIA Centaur Folate assay because serum controls may go out of range low and whole blood patient results may shift.
AlloSource, Inc. is recalling 29 units of AlloFuse DBM Putty 5cc because the donor was hemodiluted. The product is used as a bone graft extender in orthopedic applications.
Mangiacotti is recalling Ocean Hand Sanitizer Spray due to elevated counts of Serratia liquefaciens bacteria. Consumers should stop using the product.
Elgin is recalling 2013 Pelican street sweepers because seat belt buckles may fail to release, hindering emergency egress.
INO Therapeutics is recalling 22 INOmax DSIR Nitric Oxide Delivery Systems due to a software anomaly that may trigger unintended alarms.
Medtronic is recalling specific Refill Kits for implantable infusion pumps because some contain occluded extension tubing that prevents filling. No patient injuries beyond additional needle sticks have been reported.
Cabela's is recalling Electronic Jerky Blasters because the battery charger adapter can overcharge, causing the battery and adapter to overheat.
General Motors is recalling 2005-2007 Chevrolet Corvettes because a wiring issue can cause low beam headlights to fail, increasing crash risk.
Mangiacotti is recalling Pomegranate Hand Sanitizer Spray due to elevated counts of Serratia liquefaciens bacteria.
Mar Cor Purification is recalling 197 Central Water Platform (CWP) reverse osmosis systems because a specific lot of water inlet solenoid valves may fail, stopping water production.
Bausch & Lomb is recalling Biotrue Multi-Purpose Contact Lens Solution due to out-of-specification results for a disinfectant.
Wockhardt USA is recalling specific lots of Metoprolol Succinate Extended-Release Tablets because they failed dissolution testing at the nine-month time point.