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.
Nova Bus is recalling N67588 alternator cables for 2010-2014 LFS transit buses because damaged terminals may arc and cause an engine compartment fire.
Autocar is recalling 38 model year 2015 Xpeditor trucks because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.
TOR Truck Company is recalling 2008 DR8490 drilling rig carriers because a mechanical power spring may fail, preventing the accelerator pedal from returning to idle.
Highland Ridge RV is recalling 284 model year 2015 Open Range 3X trailers because defective awning screws could cause the awning to fall and injure people.
Johnson Health Tech is recalling Matrix Fitness Varsity series strength training machines because the handle attachment can detach, posing impact, laceration, and fall risks.
Volvo is recalling 2015-2016 VNX and VNL trucks because a parking brake defect may cause overheating and fire. Owners should contact dealers for inspection.
Mack is recalling 2015-2016 CXU and LEU trucks due to a parking brake defect that may cause brake drag and fire.
Great Dane is recalling 2015 Reefer and Van trailers because a brake actuator defect may cause brake drag and overheating, increasing the risk of fire.
Life Line Emergency Vehicles is recalling 2014-2015 Ford F-450 and F-550 SD emergency vehicles equipped with Liquid Spring suspension kits due to a potential mounting bracket failure.
Primal Vantage is recalling about 1,000 Ameristep Hyde tree stands because the aluminum platform can break, posing a fall risk to hunters.
Tucker Rocky is recalling specific Speed and Strength motorcycle helmets because they fail to meet federal safety standards, increasing the risk of serious injury in a crash.
Perfect Foods Bar is recalling specific lots of Peanut Butter and Cranberry Crunch nutritional bars due to potential Salmonella contamination.
Polaris is recalling 2015 Slingshot and Slingshot SL motorcycles because a steering component may fail, potentially causing loss of steering control and increasing crash risk.
Philips is recalling HeartStart MRx monitor/defibrillators because the device may malfunction, potentially delaying or disabling therapy or delivering it inadvertently.
Siemens Medical Solutions is recalling 320 linear accelerators because unauthorized third-party components may cause patient or operator injury and dose calculation errors.
House of Bricks Realty, Inc. is recalling 130 pounds of French pork rillette because the products were not presented for USDA inspection at the U.S. point of entry.
Perfect Foods Bar is recalling Peanut Butter and Cranberry Crunch bars due to potential Salmonella contamination.
Perfect Bar is recalling Cranberry Crunch nutritional bars due to potential Salmonella contamination. Consumers should stop eating the affected product.
DePuy Orthopaedics is recalling ATTUNE INTUITION Impaction Handles because the lever can fracture during knee surgery, potentially leaving device pieces in the patient.
La-Z-Boy is recalling control wands sold with Silver Luxury Lift Chairs because they can overheat and cause burns. Consumers should unplug the chair and contact a dealer for a free replacement.
Becton Dickinson is recalling specific lots of Trypticase Soy Agar and MacConkey II Agar plates due to low-level Listeria monocytogenes contamination.
Siemens is recalling 50 Artis Q and Artis Q.zen ceiling systems because suboptimal cable routing may cause wear, leading to limited functionality or system failure.
SpineFrontier, Inc. is recalling four Inline Persuader PedFuse Pedicle Screw Systems because a crack may develop in the handle, potentially progressing with continued use.
St. Jude Medical is recalling Merlin@home RF Remote Monitoring Transmitters because a software reset may cause backup operation in implanted cardiac devices.
Synthes, Inc. is recalling Malleable C-Retractors because the internal spring may corrode or fail, potentially transferring particles to patients and causing adverse tissue reactions or infection.