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.
Iowa Mold Tooling is recalling certain Series III cranes because a valve bank cover may crack and fall off, creating a road hazard.
Accuray is recalling CyberKnife Robotic systems because the gun box mounting bracket may fail, allowing the gun box to fall and contact a patient.
Del Medical is recalling VS200 radiographic cassette holders and wall stands because they can suddenly fall to the ground and contact patients.
GE Medical Systems is recalling 2,111 Mavig Monitor Suspension Systems because a reported incident involved a suspension arm falling to the floor.
Del Medical, Inc. is recalling VS300 radiographic cassette holders and wall stands because the unit can suddenly fall to the bottom of its travel and contact a patient.
Zimmer Dental Inc is recalling specific dental implants because the instructions for use omitted safety information regarding the 3.7 mmD and 4.1 mmD Trabecular Metal models.
Bearded Brothers LLC is recalling BOLD The Greek energy bars due to mold. The recall covers 150 cases distributed nationwide.
Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Zimmer Dental Inc. is recalling specific Trabecular Metal implants because safety information was omitted from the instructions for use.
Toshiba is recalling four INFX-8000V Bi-Plane X-Ray Interventional Systems because a software error caused dose data to be lost during specific imaging procedures.
Bulletproof Digital Inc is recalling FATwater Lemon bottles due to microbial growth detection. No pathogens were found.
Fagron, Inc. is recalling SyrSpend SF Suspending Base because the product contains yeast. The recall covers 88 bottles distributed nationwide.
Zimmer Dental Inc. is recalling specific dental implants because the latest instructions omitted information for certain models.
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Pharmacaribe LLC is recalling PulmoSal 7% Sodium Chloride inhalation solution because vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+).
Bulletproof Digital Inc is recalling 12,583 bottles of Berry FATwater due to microbial growth detection. No pathogens were detected.
Bearded Brothers LLC is recalling 128 cases of BOLD Coconut Curry energy bars due to mold. The product was distributed nationwide.
Merge Healthcare is recalling RadSuite picture archive systems because they may display incorrect Standardized Uptake Values (SUV). The recall covers 164 units distributed nationwide.
Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Sandoz Inc. is recalling Candesartan Cilexetil Tablets, 16 mg, because the product failed impurities and degradation specifications at a 9-month stability timepoint.
Zimmer Dental Inc is recalling specific dental implants because safety information was omitted from the instructions for use.
Bulletproof Digital Inc is recalling 5,748 bottles of Tangerine FATwater due to microbial growth detection. No pathogens were detected.
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because critical safety information was missing from the instruction manual.
Spectranetics Corp. is recalling 8 units of 2.3mm Turbo-Power OTW Manual laser atherectomy catheters because they are past their expiration date.