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.
Hino is recalling 2,641 model year 2012-2015 XJC and XFC trucks because a software issue may prevent the brake warning lamp from illuminating, increasing crash risk.
Halcore is recalling 2006 Leader Type II Ambulances equipped with specific Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.
Meijer is recalling Halloween projector flashlights because they can overheat and melt the plastic handle, posing a burn risk to users.
Morgan Olson is recalling 100 model year 2014 Mercedes-Benz Sprinter 2500 vehicles because an aluminum document holder may injure unbelted occupants in a crash.
Jaguar is recalling 2015 F-TYPE, XF, and XJ vehicles because engine components may detach, increasing the risk of fire or loss of steering.
Honda is recalling 2014 Grom125 and NSS300 motorcycles because a fuel pump bracket may swell and seize, causing the bike to stall and increasing crash risk.
BMW is recalling 223 model year 2014 i8 vehicles because a ground cable bolt may not be properly welded to the fuel tank, creating a risk of fuel leaks and fire.
Mazda is recalling 2014-2015 Mazda6 vehicles because the tire pressure monitoring system may fail to warn drivers if all four tires lose pressure simultaneously, increasing crash risk.
Murry's Inc. is recalling approximately 31,689 pounds of gluten-free breaded chicken products due to potential Staphylococcal enterotoxin contamination.
Volkswagen Group of America is recalling 2013-2015 Audi A4, S4, and Allroad vehicles because a software error may prevent front air bags from deploying in a secondary impact.
Nissan is recalling 2013 Infiniti QX56 and 2014 QX80 vehicles because the driver's air bag inflator may contain an incorrect part that could rupture during deployment.
Volkswagen is recalling 2015 Jetta and Passat vehicles because a seatback recliner bracket may not engage correctly, causing unexpected movement that could distract the driver.
Daimler Trucks North America is recalling 2015 Thomas Built Buses Saf-T-Liner HDX school buses because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
Arctic Cat is recalling approximately 40,000 model year 2008 and 2009 ATVs because front gear case components can fail, posing a crash hazard.
FDA recalls 133,930 pairs of Kendall defibrillation electrodes because they are not compatible with specific Philips AED models.
Gel Spice Co. is recalling Fresh Finds ground black pepper due to potential Salmonella contamination. Consumers should stop using the product.
FDA recalls 317,550 pairs of defibrillation electrodes because they are not compatible with Philips FR3 or FRx AEDs.
Bumble Bee Foods is recalling specific codes of Chipotle Albacore Tuna pouches because seal defects could allow contamination by spoilage organisms or pathogens.
Siemens Healthcare Diagnostics is recalling approximately 4,200 external power supply adapters for the Clinitek Status+ urine analyzer due to damage that can cause electric shock.
Coviden LLC is recalling 9,850 pairs of Medi-Trace Cadence defibrillation electrodes because they are not compatible with Philips FR3 or FRx AEDs.
Elgin is recalling 2012-2014 Broom Badger sweeper trucks because a hydraulic oil cooler fan may fail, causing overheating and potential vehicle fire.
Hospira is recalling 109,110 vials of Lidocaine Hydrochloride Injection because the product was discolored and contained visible particulates.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
The FDA is recalling 330 pairs of MediChoice Multifunction Electrodes because they are not compatible with certain Philips AED models.
Covidien is recalling Philips HEARTSTART Multifunction Electrode Pads because they are not compatible with Philips FR3 or FRx AEDs.