State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Siemens is recalling 57 SOMATOM Definition Flash CT systems in the US due to a hardware issue that may expose users to rotating or electrical parts.
Siemens Medical Solutions is recalling 57 SOMATOM Definition AS CT systems due to a hardware issue that may expose users to rotating or electrical parts.
Dorman is recalling specific aftermarket clock spring assemblies because a manufacturing defect may cause the cable to tear, preventing the driver's airbag from deploying in a crash.
Truco Enterprises is recalling On the Border Cafe Style Tortilla Chips due to possible metal fragments in the corn flour.
Aluminum Trailer Company is recalling 2016-2017 Bumper Pull Toy Haulers because the fuel tank may detach, creating a fire risk.
Stryker Howmedica Osteonics is recalling specific lots of LFIT Anatomic V40 Femoral Heads because of reported taper lock failures that caused harm.
Micro Therapeutics Inc. is recalling Marathon and UltraFlow HPC Flow Directed Micro Catheters because PTFE coating may delaminate and enter the bloodstream.
Maquet Medical Systems USA is recalling Accessory Adapter part number 600525A0 because a head rest mounted to the device slipped out of the mounting rail.
Hospira is recalling Symbiq Two Channel Infusers that may display a white screen, causing the device to stop infusion and sound an alarm, which can delay or interrupt therapy.
Trumpf Medical Systems is recalling specific operating room table tops after identifying six incidents of pinched cables.
Baxter Healthcare is recalling 22,656 Revaclear MAX dialyzers because of potential particulate matter on the blood side of the device.
Hospira is recalling 10,337 Symbiq One Channel Infusers because a software issue may cause a white screen, stopping infusion and interrupting therapy.
AtriCure, Inc. is recalling 298 AtriClip LAA Exclusion Systems due to a potential component failure that could require medical intervention.
Skidders Footwear is recalling about 5,500 children's canvas tennis shoes because sharp rivets pose a laceration hazard. Consumers should take shoes away from children and contact the company for a refund.
Brownwood Farms is recalling Cherry Butter products because they contain milk that is not declared on the label.
Brownwood Farms is recalling Cherry Raspberry Preserves because the product contains milk that is not declared on the label.
Brownwood Farms is recalling Jalapeno Cherry Butter products because they contain milk that is not declared on the label.
Reshape Medical is recalling 114 units of the Integrated Dual Balloon System Gen 1 because distillation fluid may leak during inflation.
Roche is recalling 139 COBAS INTEGRA c111 analyzers due to a software error that may cause erroneous test results.
Brownwood Farms is recalling Pear & Cinnamon Preserves because the product contains milk that is not declared on the label.
Brownwood Farms is recalling Michigan Cherry Preserves because they contain milk that is not declared on the label.
Mercedes-Benz is recalling 672 S-Class vehicles because seat belt extenders may not retract or may break in a crash, increasing injury risk.
Brownwood Farms is recalling Strawberry Preserves because the product contains milk that is not declared on the label.
Truco Enterprises is recalling On the Border Blue Corn Tortilla Chips due to possible metal fragments in the corn flour.
Becton Dickinson is recalling specific BD Spinal Anesthesia Trays because they contain Hospira 5% Lidocaine HCI ampules that are subject to a separate recall.