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.
S. Martinelli & Co is recalling 8.4 oz bottles of Sparkling White Grape due to the potential for glass fragments.
Philips is recalling ECG sync cables used with HeartStart monitors because electrical interference can cause misinterpretation of heart signals or interrupt pacing.
Columbia Northwest is recalling 2013-2014 Somerset E1 and Santa Fe trailers because the water heater may overheat, causing scalding.
National Frozen Foods is recalling Target-exclusive Italian Blend frozen vegetables due to potential Listeria monocytogenes contamination.
National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
S. Martinelli & Co is recalling Martinelli's Gold Medal Sparkling Cider due to the potential for glass fragments in the bottles.
Forest River is recalling specific 2007-2015 motorhomes because a bolt on the electric entry steps may fracture, causing the steps to become unstable and increasing the risk of injury.
National Frozen Foods Corporation is recalling Monarch and Valmont Italian Vegetable Blend due to potential Listeria monocytogenes contamination.
Downing Labs, LLC is recalling Taurine Injectable, 50mg/mL, 30mL vials due to a lack of assurance of sterility. The recall affects 123 vials distributed nationwide and internationally.
Civco Medical Instruments is recalling 54 boxes of Large Gauge Infiniti Plus Needle Guides because the sterility of the product cannot be assured.
National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Civco Medical Instruments is recalling 717 boxes of Infiniti Plus Needle Guides because the sterility of the product cannot be assured.
Civco Medical Instruments is recalling 1,139 boxes of Biopsy Starter Kits because the sterility of the product cannot be assured.
Newmar is recalling 2016 King Aire vehicles that may lack a required emergency exit window over the driver's side dinette table, potentially delaying escape during an emergency.
US Compounding Inc is recalling 1,421 vials of Lincomycin/Lidocaine due to deficient practices that may impact sterility assurance.
TZ Medical Inc. is recalling Neptune Plus hemostasis pads because the instructions for use do not match the original FDA submission.
Vintage Pharmaceuticals is recalling 912 bottles of 12.5 mg Hydrochlorothiazide capsules because of the presence of particulate matter.
Ameditech is recalling specific Immutest drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and in Australia.
Ameditech is recalling 787 kits of 1 Step 12 Panel Cup drug tests due to reduced reactivity. The products were distributed in the US and Australia.
Ameditech is recalling iCup drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.
Ethicon Endo-Surgery is recalling Harmonic ACE+ 7 Laparoscopic Shears because holes in the Tyvek packaging can compromise the sterile barrier.
Par Pharmaceutical is recalling Meclizine Hydrochloride Tablets because they failed impurity specifications. The recall covers 100 and 1000-count bottles distributed nationwide.
Ameditech is recalling 11 Panel Drug Abuse Tests because they have shown reduced reactivity. The affected products are distributed in the US and Australia.
Ameditech is recalling ArcPoint Labs 10 Panel Dip Screen (OXY) drug tests because they have shown reduced reactivity.
Ameditech is recalling ProScreen drug panel tests because they have shown reduced reactivity. The recall covers 31,530 units distributed in the US and Australia.