State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
JD & SN Inc. is recalling 13 vials of 80 mg testosterone pellets because the FDA cannot ensure the sterile compounded drugs are free from contamination.
Kermit, Inc. is recalling 12-ounce bottles of Key Lime Cocktail Sauce due to undeclared soy on the label.
Encore Medical is recalling 277 Turon Shoulder Impaction Fixtures because polymer material wore off during assembly, potentially contaminating the implant.
Kermit, Inc. is recalling Kermit's P4 Hot Sauce because the product label fails to declare soy, a major food allergen.
Kermit, Inc. is recalling 16 oz bottles of Key Lime Barbecue Sauce due to undeclared soy on the label.
Abbott Laboratories is recalling 65 ARCHITECT i2000SR diagnostic systems worldwide because they contain incorrect tubing.
Encore Medical is recalling 634 units of Reverse Shoulder Prosthesis Stem Impaction Fixtures because polymer wear from the fixtures can damage the titanium coating on humeral stems during assembly.
Synthes (USA) Products LLC is recalling 25 units of Threaded Plate Holders that are incorrectly etched with the wrong part number and may not fit into a Small Fragment Plate.
Philips Medical Systems is recalling 109 Ingenuity Core 128 CT systems due to X-ray measurement errors causing image artifacts.
Sentinel CH SpA is recalling 765 kits of Sentinel MULTIGENT Ammonia Ultra Reagent because results may be below the linear range for samples collected in heparin tubes.
Philips Medical Systems is recalling 108 Brilliance 64 CT systems worldwide due to an X-ray measurement error that causes Ring/Dot artifacts.
Philips is recalling 36 Ingenuity Core CT systems worldwide due to an X-ray measurement error that causes Ring/Dot artifacts in images.
Philips Medical Systems is recalling 323 Brilliance 16-Slice CT systems worldwide due to X-ray measurement errors causing Ring/Dot artifacts.
Varian Medical Systems is recalling ARIA Radiation Oncology software versions 10, 11, 13.0, and 13.5 because admin instructions may fail to print or transmit.
Philips Medical Systems is recalling 67 Ingenuity Flex CT systems worldwide due to an X-ray measurement error that causes Ring/Dot artifacts in images.
Becton, Dickinson and Company is recalling two lots of BD CD3 (SK7) FITC in vitro diagnostic reagents due to an error in the Spanish small text on the label.
Prevost is recalling 2016 H3-45 and X3-45 VIP coaches because front suspension studs may fail, allowing a wheel to turn unexpectedly and increasing crash risk.
Newmar is recalling 60 recreational vehicles due to a potential ABS modulator valve fracture that could impair braking performance.
GE is recalling about 33,500 Zoneline air conditioning and heating units due to a risk of fire caused by moisture accumulation and electrical arcing.
Toyota is recalling 2013-2015 Avalon and Lexus ES vehicles because the Pre-Collision System may unexpectedly brake when detecting steel road objects.
Forest River is recalling 217 model year 2016 recreational vehicles because an incorrect shift cable bracket allows the vehicle to be shifted out of park without applying the brakes.
Diamond Coach is recalling 49 model year 2006-2011 PT and VIP transit buses equipped with certain Ricon wheelchair lifts. The lifts may have oversized pivot holes that allow bearings to move, potentially causing the platform to fall out of the vehicle.
Carra Imports is recalling about 55,500 custom window shades due to a strangulation hazard involving continuous loop cords or exposed inner cords.
KME is recalling 2016 Predator and Severe Service vehicles because improperly tightened axle hex nuts may cause the driveshaft to disconnect, increasing crash risk.
Indian Motorcycle is recalling 7,614 motorcycles from 2015-2016 because a rear brake master cylinder defect may cause a loss of braking power.