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.
Prevost is recalling 291 motorcoaches because certain fire extinguishers may not fully discharge, increasing injury risk during a fire.
Oscar's Hickory House Inc. is recalling approximately 32 pounds of beef jerky due to a processing deviation that makes the product susceptible to environmental pathogens.
General Motors is recalling 2015 Chevrolet Cruze vehicles because parking brake cable brackets may not be properly fastened, increasing the risk of the vehicle rolling away.
Chrysler is recalling 2015 Dodge Charger and Challenger SRT vehicles because a fuel rail hose may leak, increasing the risk of a vehicle fire.
Chrysler is recalling 2012-2013 Jeep Grand Cherokee and Dodge Durango vehicles because a fuel pump relay may fail, causing the vehicle to stall without warning and increasing crash risk.
Blue Bird is recalling 2016 All American transit buses because a steering shaft clamp may contact the rubber boot, increasing steering effort and crash risk.
Nissan is recalling 2013-2015 Altima vehicles because the secondary hood latch may fail to engage, allowing the hood to open while driving.
Kawasaki is recalling 194 police-modified 2009-2013 Concours 14 motorcycles because added wiring may cause the main fuse to blow, leading to engine stalling and crash risk.
GE Healthcare is recalling MRI systems because a disconnected MRU could delay the removal of ferrous objects, posing a life-threatening injury risk.
Hospira Inc. is recalling 142,644 bags of Lactated Ringer's and 5% Dextrose Injection USP due to confirmed mold particulates in the solution.
Hospira Inc. is recalling 2,500 vials of Propofol Injectable Emulsion because the products experienced uncontrolled temperature excursions during transit.
McNeilus is recalling 2005-2014 Bridgemaster V Mixers because the optional parking brake system may fail to maintain required pressure, increasing crash risk.
Mako Surgical Corporation is recalling 228 units of the Restoris Partial Knee Application RIO because the surgical burr may continue spinning outside the intended boundary after controls are released.
Hospira is recalling specific vials of 1% Lidocaine Hydrochloride Injection because a returned sample contained human hair attached to the stopper.
CME America is recalling BodyGuard and BodyGuard 323 infusion pumps due to a potential for over-delivery of medication.
Probar LLC is voluntarily recalling specific lots of Frosted Peanut Butter BASE Protein Bars due to the possible presence of an undeclared milk allergen.
Cosco is recalling about 273,000 convertible hand trucks because wheel hubs can break and eject pieces, posing an injury risk.
Hickory Springs is recalling specific RV quad entry steps because rivets may shear, causing steps to fail and occupants to fall.
Nidek Inc is recalling 16 MC-500 Multicolor Laser Photocoagulators because the spot size control may turn by itself, posing a risk of unintended laser delivery.
Farber Specialty Vehicles is recalling specialty vehicles equipped with Ricon wheelchair lifts because the platform side plates may crack, posing a risk of injury.
Terumo is recalling 103 HX2 Temperature Management Systems because a malfunctioning mixing valve can cause loss of cooling or heating capability during surgery.
Teleflex is recalling RUSCH Curved Reinforced Endotracheal Tubes because the labeled cuff diameter does not match the actual cuff diameter, though the actual product meets specifications.
Hospira Inc. is recalling specific lots of Vancomycin Hydrochloride for Injection because they experienced uncontrolled temperature excursions during transit.
Cincinnati Sub-Zero is recalling CT-99 cold therapy pads because seals may separate during use, causing water leaks.
Pulsion Medical Inc is recalling 90 units of the Pulsiocath PiCCO ProAQT Monitoring Kit due to cracks and holes found in the primary packaging.