State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Newly Weds Foods is recalling Breader X1 due to potential undeclared milk. The product was distributed nationwide, in Mexico, and Canada.
Becton Dickinson is recalling 22,400 units of 5ml syringes because several lots did not receive the specified dose of irradiation required to meet sterility standards.
Newly Weds Foods is recalling 25,300 lbs of Batter Mix because it may contain undeclared milk, posing a risk to individuals with milk allergies.
Newly Weds Foods is recalling 810,500 lbs of Breader products because they may contain undeclared milk, posing a risk to individuals with milk allergies.
Newly Weds Foods is recalling Breader X1 because it may contain undeclared milk. The product was distributed nationwide and to Canada and Mexico.
Newly Weds Foods is recalling Breader X1 because the product may contain undeclared milk. The recall covers 1,175 lbs distributed nationwide, in Mexico, and Canada.
Newly Weds Foods is recalling Fine Cracker Meal because it may contain undeclared milk. The product was distributed nationwide and in Mexico and Canada.
Newly Weds Foods is recalling B30352 Breaders X1 nationwide and in Canada and Mexico due to potential undeclared milk.
Newly Weds Foods is recalling Breader X5 because it may contain undeclared milk. The product was distributed nationwide and to Canada and Mexico.
Newly Weds Foods is recalling Breader X2 because it may contain undeclared milk. The product was distributed nationwide and in Mexico and Canada.
Newly Weds Foods is recalling 10,300 lbs of Batter Mix X1 because it may contain undeclared milk. The product was distributed nationwide and in Mexico and Canada.
Newly Weds Foods is recalling 2,500 lbs of Breader X1 because the product may contain undeclared milk. The recall covers distribution in the US, Mexico, and Canada.
Newly Weds Foods is recalling Breader X1 because it may contain undeclared milk. The product was distributed nationwide and in Mexico and Canada.
Newly Weds Foods is recalling Breader X2 products because they may contain undeclared milk, posing a risk to individuals with milk allergies.
Newly Weds Foods is recalling 17,900 lbs of Batter Mix because it may contain undeclared milk. The product was distributed nationwide and in Mexico and Canada.
Newly Weds Foods is recalling BREADER X3 because the product may contain undeclared milk. The recall covers 244,000 lbs distributed nationwide and in Mexico and Canada.
Newly Weds Foods is recalling Breader X2 because it may contain undeclared milk. The product was distributed nationwide and to Mexico and Canada.
Newly Weds Foods is recalling specific lots of BATTER MX X3 because the product may contain undeclared milk. The recall covers 211,450 lbs distributed nationwide and in Mexico and Canada.
Newly Weds Foods is recalling 2,500 lbs of Batter Mix X1 because it may contain undeclared milk. The product was distributed nationwide and in Mexico and Canada.
Newly Weds Foods is recalling 194,640 lbs of Predust X1 seasoning because it may contain undeclared milk, posing a risk to individuals with milk allergies.
Teva Pharmaceuticals is recalling Buprenorphine and Naloxone Sublingual Tablets because test results showed out-of-specification impurities.
Pentax Medical is recalling 241 laryngeal strobe systems because they were not always provided with required 9175 isolation transformers.
Pentax of America is recalling 241 units of 9310HD Digital Video Capture Modules because they were not always provided with required 9175 isolation transformers.
Hospira is recalling 701 vials of Argatroban Injection because a denitroquinoline-related impurity exceeded specifications during testing.
Shionogi Inc. is recalling Mefenamic Acid 250mg capsules because stability testing showed low dissolution results.