State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jayco is recalling 2,747 model year 2013-2015 Seismic and Eagle Premier trailers because entry step rivets may shear, causing steps to fail and occupants to fall.
FMF Store Fixtures Inc. is recalling specific Nu-Line and Fleetline fender brackets and kits due to insufficient welds that may cause fenders to detach.
Snow Peak is recalling about 220 Japanese Axe M units because the handle can crack, allowing the axe head to come loose and posing a laceration or impact hazard.
Sabra Dipping Company is recalling 10 oz Classic Hummus after a Michigan sample tested positive for Listeria monocytogenes.
Sabra Dipping Company is recalling 30 oz Classic Hummus after a Michigan sample tested positive for Listeria monocytogenes.
Hospira is voluntarily recalling specific lots of Ketorolac Tromethamine Injections because of crystallization. The affected products were distributed nationwide, in Puerto Rico, and in Guam.
Navajo Agricultural Products Industry is recalling Navajo Pride Bleached All Purpose Flour due to Salmonella contamination.
Sabra Dipping Company is recalling 32-ounce containers of Classic Hummus without Garnish after a sample tested positive for Listeria monocytogenes.
Sabra Dipping Company is recalling Sabra Classic Hummus after a sample tested positive for Listeria monocytogenes. The product was distributed nationwide.
Sabra Dipping Company is recalling specific tubs of Roasted Garlic and Classic Hummus after a Michigan sample tested positive for Listeria monocytogenes.
Hope Foods is voluntarily recalling one lot of Kale Pesto Hummus because it contains undeclared walnuts. Consumers should check for the specific lot code and UPC.
Teva Pharmaceuticals USA is recalling specific lots of Fluoxetine Capsules USP, 20 mg, due to an elevated level of a residual solvent impurity in the active pharmaceutical ingredient.
Dako North America is recalling the Test Request Distributor software module for the Dako Omnis System because it may execute the wrong test after a user updates a request.
Cuisine Innovations is recalling Black Bean Burgers because they may contain undeclared peanut protein. The product was distributed nationwide.
Vital Signs Colorado is recalling LightWand Stylets because sterile packaging may be breached without visible signs, posing a patient safety risk.
Lumenis is recalling 117 Light Sheer Desire Diode Laser Systems because software parameters exceed manual settings, potentially causing burns.
Cuisine Innovations is recalling Guiltless Gourmet Southwestern Veggie Burgers because they may contain undeclared peanut protein.
The Anspach Effort, Inc. is recalling Synthes Small Battery Drive Oscillating Saw Attachments because they may disengage during surgery, posing a risk of injury.
Steris is recalling 491 Caviwave Pro Ultrasonic Cleaning Systems because a power interruption may stop the pump and generator without alerting the user.
Cuisine Innovations LLC is recalling Southwestern Veggie Burgers because they may contain undeclared peanut protein.
Cuisine Innovations LLC is recalling Chef's Line Black Bean Burgers because they may contain undeclared peanut protein.
Vital Signs Colorado is recalling LightWand Stylets because sterile packaging may be breached without visible signs, posing a patient safety risk.
Spacelabs is recalling Ultraview SL Command Modules upgraded with the Masimo SpO2 Option because monitoring suspends for approximately 10 seconds during resets.
Amtryke LLC is recalling 53 Model 1424 Community Cruiser Hand Cycles due to complaints of cracked frames. The recall covers units distributed nationwide to 18 states.
Fresenius Medical Care is recalling 2008K2 hemodialysis machines because the GranuFlo acetate value is incorrectly displayed as 4mEq/l instead of 8mEq/l on the Select Concentrate screen.