State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Vans is recalling about 2,400 boy's hooded jackets because the hood drawstrings pose a strangulation hazard to young children.
Lippert is recalling 2006-2013 travel trailer doors with Fastec deadbolts that may jam, potentially trapping occupants inside the vehicle.
Conagra is recalling specific lots of P.F. Chang's Pork & Leek Dumplings because they were inadvertently packaged with Shrimp & Pollack Fish dumplings, resulting in undeclared allergens.
Chrysler is recalling 2013 Dodge Avenger, Chrysler 200, and 2014 Jeep Compass and Patriot vehicles due to abrasive debris in engine bearings that may cause oil pressure loss and engine failure.
Pentax Medical is recalling 76 OF-B194 Gas/Water Feeding Valves due to a manufacturing defect that may cause improper CO2 gas stoppage during endoscopic procedures.
Chrysler is recalling specific Dodge Ram trucks because the left tie rod assembly may break, potentially causing a loss of steering control and increasing crash risk.
Hyundai is recalling 21,207 2007-2008 Entourage vehicles because front lower control arms may fracture due to corrosion, increasing the risk of a crash.
Synthes USA HQ, Inc. is recalling 319 units of the Sternal Zip Flex System because the application instrument may cut the implant, leading to loosening.
Chrysler is recalling specific 2008-2012 Dodge RAM trucks because the left tie rod assembly may break, potentially causing loss of steering control and increasing crash risk.
Atossa Genetics is recalling ForeCYTE Breast Health Test kits due to FDA concerns regarding instructions for use and promotional claims.
Chrysler is recalling 2008-2012 RAM 4500 and 5500 trucks because the left tie rod assembly may break, potentially causing loss of steering control.
Edwards Lifesciences is recalling EMBOL-X Glide Protection Systems because the cannula tip may deform. The recall covers 12,034 units distributed in the US and Canada.
Medtronic is recalling Activa PC and RC deep brain stimulators due to a potential for overstimulation or stimulation in the wrong area during device recovery.
Siemens is recalling RAPIDLab and RAPIDPoint blood gas analyzers because users can enter wrong patient IDs, risking sample misidentification.
Globus Medical is recalling MicroFuse Putty because the sterility assurance level cannot be verified. The product is a bone graft extender used in medical procedures.
Toshiba is recalling 477 Xario XG Diagnostic Ultrasound Systems because the transducer head may overheat during specific imaging modes.
GE Healthcare is recalling Centricity PACS-IW software due to issues that could display incorrect patient images or under-report dose values, posing a safety risk to patients.
Xoran Technologies is recalling Minicat CT Scanners that failed to meet specifications for dose rate, potentially affecting patient safety.
Siemens Healthcare Diagnostics Inc. is recalling RAPIDPoint 400 series blood gas analyzers because users may enter incorrect patient IDs, leading to sample misidentification.
Xoran Technologies is recalling 320 MiniCAT CT Scanners because the gantry may fail to rotate while emitting radiation.
DePuy Spine is recalling 102 units of Pipeline LS Dilators and Holding Clips because they were used for neuromonitoring, a function for which the devices are not FDA cleared.
Siemens is recalling RAPIDPoint 405 blood gas analyzers because users may enter incorrect patient IDs, leading to sample misidentification.
Chrysler is recalling 2013 Dodge Dart vehicles because front seat side airbags may not be properly installed, potentially failing to deploy in a crash.
Toshiba is recalling 427 Aplio MX Diagnostic Ultrasound Systems because the transducer head may overheat during specific imaging modes.
Toshiba is recalling 17 diagnostic ultrasound systems because the transducer head may overheat under specific operating modes, posing a burn risk to patients.