State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Gree Electric Appliances is recalling approximately 2.5 million dehumidifiers sold under various brands because they can overheat and catch fire, posing serious fire and burn hazards.
Stanley is recalling about 70,000 commercial door locksets because the latches can fail, preventing doors from being unlocked from the inside during an emergency.
Toyota is recalling 2011-2016 Sienna minivans because the power sliding door may open unexpectedly while the vehicle is moving, increasing the risk of injury to occupants.
Forest River is recalling 2016-2017 StarTrans PS2 buses because the instrument cluster may display 'PARK' instead of 'BRAKE' during a brake malfunction, increasing crash risk.
Johnson Health Tech is recalling Matrix ClimbMills because the stop/pause controls can malfunction, posing a fall hazard to users.
Autocar is recalling 2013-2017 Xpeditor vehicles because fuse box vibration may cause the ignition relay to open, leading to an engine stall and increased crash risk.
Midwest Automotive Designs is recalling 2016 Mercedes-Benz Sprinter 2500 and 3500 vans because certain left seat adjusters may allow seats to move during a crash.
Autocar is recalling 2012-2016 Xpeditor vehicles because hybrid power drive unit bolts may not be tightened properly, risking detachment and crashes.
Maserati is recalling 326 model year 2017 Quattroporte and Ghibli vehicles because a loose rear differential pinion nut may cause the rear wheels to lock up, increasing crash risk.
KTM is recalling specific 2013-2016 Adventure and Super Adventure motorcycles because a fraying wiring harness can melt the brake line, potentially causing brake failure.
Gulf Stream is recalling 2016-2017 Conquest and B Touring Cruiser motorhomes because the in-dash radio assembly was improperly wired, allowing the DVD to operate while the vehicle is in motion.
National Steak and Poultry is recalling approximately 17,439 pounds of ready-to-eat chicken products that may be undercooked, posing a risk of bacterial pathogens.
Kalmar is recalling 798 model year 2014-2016 Ottawa T2 vehicles because an overloaded ground circuit may increase the risk of a dashboard fire.
Sandoz Inc. is recalling L-Cysteine Hydrochloride Injection vials because an FDA inspection raised concerns that the product's sterility may be compromised.
ICU Medical is recalling 205 SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.
Siemens Healthcare Diagnostics is recalling 448 Aptio Automation Modules because power cord plugs may overheat when connected to FlexLab and Aptio systems.
Sandoz Inc. is recalling L-Cysteine Hydrochloride Injection because an FDA inspection raised concerns that the product's sterility may be compromised.
ICU Medical is recalling 40 Pediatric CVL Monitoring Kits containing Transpac IV transducers due to a potential for leak.
Work 'N Leisure is recalling Practi-VALVE training valves because the end-cap can detach in a user's mouth, posing a choking hazard.
ICU Medical is recalling specific SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.
Siemens is recalling Artis zee/zeego angiographic x-ray systems because the semi-automatic focus switch may fail when the footswitch is pressed multiple times.
ICU Medical is recalling 160 units of Transpac IV transducer kits due to a potential leak. The affected products were distributed nationwide.
ICU Medical is recalling Transpac IV bifurcated monitoring kits because of a potential for leak in the SafeSet Reservoir and blood sampling components.
ICU Medical is recalling specific Transpac IV monitoring kits because of a potential leak in the SafeSet Reservoir and blood sampling components.
Mevion Medical Systems is recalling six MEVION S250 proton radiation therapy units because completing setup without a program move can cause an isocenter error.