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.
Neely Coble is recalling 52 Isuzu NQR vehicles with dual steering modifications due to a potential steering column separation risk.
Intuitive Surgical is recalling 1,034 EndoWrist Stapler 45 instruments because they may not be removable from tissue.
FDA recalls 31,590 pairs of Kendall defibrillation electrodes because they are not compatible with Philips FR3 or FRx AEDs.
Bumble Bee Foods is recalling Sun Dried Tomato pouches because seal defects could allow contamination by spoilage organisms or pathogens.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna due to seal defects that could allow contamination by spoilage organisms or pathogens.
Siemens Healthcare Diagnostics is recalling external power supply adaptors for the Clinitek Status urine analyzer because they are damaged and can cause electric shock.
Merge Healthcare is recalling eFilm Workstation versions 4.0 and 4.0.1 because a software defect may cause users to select the wrong patient study when using the thumbnail panel.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Biomet is recalling six Discovery Elbow Humeral Trials that were incorrectly manufactured as left-sided but etched as right-sided.
Gulf States Toyota is recalling 142 model year 2015 Toyota Tacoma vehicles because they may have incorrect load carrying capacity labels, which could lead to vehicle overload.
Siemens Healthcare Diagnostics is recalling external power supply adaptors for the Clinitek Status urine analyzer due to damage that can cause electric shock.
Arrow International is recalling Select Kits and Maximal Barrier Precautions Kits containing BD Posiflush syringes because open seals may compromise sterility.
Bumble Bee Foods is recalling Jalapeno Albacore Tuna pouches due to seal defects that could allow contamination by pathogens.
Spartan Motors is recalling 2010-2015 Gladiator vehicles because the engine cooling fan may break during severe vibration, posing an injury risk if the hood is open.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Primus Medical LLC is recalling 1,726 AC powered adjustable bed frames used in nursing facilities because the head deck actuator bracket may separate from the frame.
Intuitive Surgical is voluntarily correcting labeling and software for the EndoWrist One Vessel Sealer used with the da Vinci Si Surgical System.
Kraft Heinz Foods is voluntarily recalling 7,691 cases of American cheese slices because a supplier failed to store an ingredient at the correct temperature.
Valeant Pharmaceuticals is recalling 34,218 tubes of Hydrocortisone Butyrate Cream 0.1% because the product failed stability testing for potency and preservative levels.
Valeant Pharmaceuticals is recalling 1,663 tubes of Locoid cream because the active ingredient and preservatives were subpotent at the 18-month stability test point.
Roche Diagnostics is recalling Omni Micro-electrodes for the cobas b221 analyzer because default reference values are inconsistent with other instruments and instructions.
Zydus Pharmaceuticals is recalling Topiramate 200 mg tablets because 100 mg tablets were found mixed in the bottles.
Gyma Laboratories of America, Inc. is recalling Clonidine Base Micronized due to lack of good manufacturing practices identified by the Italian Medicines Agency.