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 Products, Inc. is voluntarily recalling Mojo Risen because FDA testing found undeclared sildenafil, an active ingredient in erectile dysfunction drugs.
American Health Packaging is recalling Oxcarbazepine Tablets due to a label mix-up with Ibuprofen tablets.
Baxter Healthcare is recalling 171,672 bags of Potassium Chloride Injection due to the presence of particulate matter, including fibers and plastics.
Nova Products, Inc. is voluntarily recalling XZONE GOLD capsules because FDA testing found undeclared sildenafil and tadalafil.
General Motors is recalling 2013-2015 Chevrolet Sparks because the secondary hood latch may corrode, potentially allowing the hood to open while driving.
Polar Tank is recalling 2014 SRJ7 trailers because suspension pivot bolts may fail, causing the axle to separate and increasing crash risk.
Daimler Trucks North America is recalling 2014-2015 FCCC truck chassis because improperly secured propane fuel injectors or leaking tubes may cause a stall or fire.
Nestle USA is recalling Lean Cuisine Chicken with Peanut Sauce due to package mislabeling regarding peanut content.
Nova Products, Inc. is voluntarily recalling XZone 1200 capsules because FDA analysis found undeclared sildenafil and tadalafil.
Vibrant Health is recalling Green Vibrance dietary supplements because a raw material used in manufacturing was found to contain Salmonella bacteria.
Vibrant Health is recalling Green Vibrance dietary supplement powder because a raw material used in its manufacture was found to contain Salmonella bacteria.
Data Innovations, LLC is recalling ProVue Instrument Driver for JResultNet versions 1.5.3 and below because the software may misassociate data with patient results.
JK Products & Services is recalling 1,948 Sun Dash Radius 252 tanning beds because excessive flexing of the main electrical cord can compromise wire integrity.
Varian Medical Systems is recalling 512 4D Integrated Treatment Consoles because user error can allow improper clearing of safety interlocks.
Bio-Detek is recalling 198 cases of ZOLL Pro-padz Sterile Adult Multi-Function Electrodes because the sterility of the devices is not assured.
Varian Medical Systems is recalling C-Series High Energy Linear Accelerators due to a trend of unexpected decreases in beam output during 6MV photon treatment.
Volcano Corporation is recalling TrakBack II Disposable Pullback Devices because internal testing identified a potential breach to the sterile barrier that may impact product sterility.
Becton Dickinson is recalling specific lots of Vancomycin Screen Agar because the product may allow susceptible bacteria to grow, leading to false resistance test results.
Bio-Detek is recalling ZOLL Pro-padz Sterile Adult Multi-Function Electrodes because the sterility of the devices is not assured.
Elkhart Coach is recalling 2006-2014 Ford E-350 and E-450 vans equipped with specific Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.
Hospira Inc. is recalling 75,000 vials of Bupivacaine Hydrochloride 0.5% due to a confirmed report of a brown, rust-colored particle embedded in the glass vial.
Bio-Detek, Inc. is recalling ZOLL Pro-padz Sterile Adult Multi-Function Electrodes because the sterility of the devices is not assured.
Siemens is recalling ADVIA Chemistry A1c_3 Calibrators because they may cause a percent bias in HbA1c test results.
ArjoHuntleigh is recalling Tenor mobile passive lifts because the spreader bar bolt may break during use, posing a risk to patients and caregivers.
Bard Peripheral Vascular Inc is recalling Bard DuaLok Breast Lesion Localization Wires because portions of the wire may protrude from the packaging, breaching the sterile barrier.