State
73,503 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sutphen is recalling 2019-2020 fire trucks because a disabled sleep mode causes the wireless remote controller's batteries to discharge faster than normal.
Pentax of America Inc. is recalling 108 Pentax Medical Video Duodenoscopes because the distal end cap may detach during procedures, posing risks of injury or aspiration.
Welch Allyn is recalling ProBP 3400 Digital Blood Pressure Devices due to a risk of fluid ingress causing electrical shorts and potential shock.
James Leckey Design Ltd is recalling 2,719 MyWay Walker Chassis units because weld failures caused casters to detach from the rear legs.
Dentech Corp. is recalling 87,842 units of KSK Rubber Dam Clamps because they may break during use. The recall covers units distributed in the US and worldwide.
Daimler Vans USA is recalling 2019-2021 Mercedes-Benz and Freightliner Sprinter vans because a software defect may cause the rearview camera image to fail to display.
Philips is recalling three IntelliVue MX40 patient monitors because manufacturing process failures may have resulted in defective devices.
USDA FSIS issued a public health alert for frozen raw breaded stuffed chicken products due to a Salmonella Enteritidis illness cluster. Consumers are advised to cook products to 165 F.
Volvo Trucks is recalling certain 2021-2022 VAH, VDH, VNL, and VNR vehicles due to a defective hubcap compression spring that can cause the hubcap to separate, creating a road hazard. Dealers will remove the hubcap free of charge.
Nobel Biocare Procera LLC is recalling specific implant crown units because they were not manufactured to specification. The recall affects units distributed in the US and several international countries.
Roche Diagnostics is recalling 20,468 Iron Gen 2 reagent cassettes because they may produce discrepant elevated results on specific analyzers.
Nobel Biocare Procera LLC is recalling specific implant crowns because they were not manufactured to specification. The recall affects units distributed in the US and several international countries.
Siemens Healthcare Diagnostics is recalling the Centaur Syphilis Assay-SYP Kit due to potential carryover into other assays on specific systems.
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because customer complaints regarding ripped patches and adhesive transfer exceeded action limits.
Nobel Biocare Procera LLC is recalling seven implant crown units because they were not manufactured to specification. The recall covers distribution in the US and several international countries.
Brew Dr. Uplift Blood Orange Lemon drink is being recalled because yeast was found in the shelf-stable cans.
Brew Dr. Uplift Blueberry Raspberry Yerba Mate is being recalled because yeast was found in the shelf-stable cans.
Brew Dr. Uplift Mango Passionfruit drinks are being recalled because yeast was found in the product. Consumers should stop drinking the affected cans.
Ortho-Clinical Diagnostics is recalling 74 units of VITROS CoV2 Ag calibrator (Lot 0020) due to potential unexpected calibration failures.
Brill Inc is recalling specific batches of baked chocolate chip cookies due to the potential presence of small foreign objects.
Nobel Biocare Procera LLC is recalling specific implant crown units that were not manufactured to specification. The recall affects units distributed in the US and several international countries.
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because customer complaints regarding ripped patches and adhesive issues exceeded action limits.
Nobel Biocare Procera LLC is recalling two dental implant crown units because they were not manufactured to specification. The affected units were distributed in the US and several international countries.
Ascend Laboratories LLC is recalling 34,296 bottles of Olmesartan Medoxomil 20 mg tablets because they may contain a foreign tablet or capsule.
Dr. Reddy's Laboratories is recalling Atorvastatin Calcium 10 mg tablets due to the presence of degradation impurities.