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.
Ameritrans is recalling 2015-2016 285 shuttle buses because wheelchair lift platform side plates may crack or bearings may shift, posing an injury risk.
LaRose Industries is recalling Cra-Z-Jewelz jewelry kits because the slider bracelet component contains high levels of lead, posing a health risk to young children.
Southeast Toyota Distributors is recalling specific Toyota vehicles equipped with aftermarket seat heaters due to a risk of electrical short circuits and fire.
Debco Bag is recalling Tonal Thirst ceramic mugs because the handles can break, posing burn and laceration risks to consumers.
Daimler Trucks North America is recalling specific Thomas Built Buses because corrosion on the emergency door handle stem may delay evacuation during an emergency.
The Sausage Maker, Inc. is recalling Dried Sausage Sticks seasoning because the Fermento ingredient contains undeclared whey protein and skim milk powder.
Master Herbs is recalling Licorice Coughing Liquid because it contains undeclared morphine and was marketed without an approved NDA or ANDA.
R Thomas Marketing, LLC is recalling Weekend Prince capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Baxter Healthcare is recalling 273,520 bags of 0.9% Sodium Chloride Injection USP due to the presence of cardboard particulate matter.
R Thomas Marketing, LLC is recalling Hard Ten Days capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Tiger King capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Samurai-X capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
The FDA is recalling 'Bigger Longer More Time More Sperms' because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Lipo Escultura capsules are being recalled because they contain sibutramine and diclofenac, making them unapproved drugs rather than dietary supplements.
R Thomas Marketing, LLC is recalling Stree Overlord capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
AmEx Pharmacy is recalling 836 Avastin syringes nationwide because testing revealed bacterial contamination.
Baxter Healthcare Corp. is recalling 334,560 bags of Metronidazole Injection USP due to the presence of a cloth fiber. The product was distributed nationwide and in Puerto Rico.
The Sausage Maker, Inc. is recalling Trail Bologna seasoning because it contains undeclared whey protein and skim milk powder.
Lucy's Weight Loss is recalling Shorts on The Beach Strong Formula capsules nationwide because they contain undeclared sibutramine and phenolphthalein.
R Thomas Marketing, LLC is recalling Black Ant King capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Centro Naturista is recalling Smart Lipo Dietary Supplement capsules because they contain undeclared sibutramine, desmethylsibutramine, and phenolphthalein.
R Thomas Marketing, LLC is recalling Germany Niubian capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Sanofi-Aventis is recalling 159,000 Auvi-Q epinephrine auto-injectors nationwide because a defective delivery system may result in inaccurate dosage delivery.
Lucy's Weight Loss System is recalling Shorts on the Beach capsules because they contain undeclared Sibutramine, Phenolphthalein, and/or Diclofenac.
Baxter Healthcare is recalling 7,436 bags of Clinimix E injection due to the presence of dried skin particulate matter. The product was distributed nationwide and in Puerto Rico.