The Recall Desk

State

US Virgin Islands product recalls

73,576 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
178
Critical
12
Severe
39
Most recent
2026-10-21

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.

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27351–27375 of 73754

  • HighNHTSA·20V645000·2020-10-19

    Mitsubishi Fuso Trucks Recalled for Brake Booster Vacuum Pump Defect

    Mitsubishi Fuso is recalling 2019-2021 FEC7T, FEC9T, and FECZT trucks because heat from the exhaust manifold may crack the brake booster vacuum pump diaphragm, potentially disabling power brake assist.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC7T, FEC9T, FECZT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V644000·2020-10-19

    Audi Recalls One 2020 Q3 for Driver's Seat Frame Bolt Defect

    Audi is recalling one 2020 Q3 because the driver's seat frame may be incorrectly bolted to the seat rail, increasing injury risk in a crash.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E079000·2020-10-17

    Fuel Delivery Module Recall Due to Potential Stalling Risk

    Continental Automotive Systems is recalling Vitesco NG2 Fuel Delivery Modules where a plastic burr may block the mixing tube, causing insufficient fuel supply and vehicle stalling.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E078000·2020-10-16

    Weldon V-Mux Vista IV LCD Displays Recalled for Electrical Lockup

    Akron Brass is recalling Weldon V-Mux Vista IV LCD displays used in emergency vehicles because they may lock up due to voltage spikes, potentially delaying emergency efforts.

    Product
    ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V639000·2020-10-15

    GM Recalls 2020 SUVs for Fuel Pump Defect Causing Engine Stalls

    General Motors is recalling 2,781 2020 Buick, Cadillac, Chevrolet, and GMC SUVs because a fuel pump defect may cause the engine to stall without warning.

    Product
    CADILLAC — CADILLAC, BUICK, CHEVROLET XT5, XT6, ENCLAVE, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V582000·2020-10-15

    Prime-Time Recalls 2014-2019 Ram ProMaster Paratransit Vehicles

    Prime-Time Specialty Vehicles is recalling 2014-2019 Ram ProMaster Paratransit vehicles because the transmission shifter cable may disconnect, causing unintended movement.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V638000·2020-10-15

    GM Recalls 2014-2016 Chevrolet SS and Caprice PPV for Seat Belt Defect

    General Motors is recalling 1,788 vehicles because a previous repair may have been improper, causing the driver's seat belt tensioner cable to fatigue and separate.

    Product
    CHEVROLET — CHEVROLET CHEVEROLET SS, CAPRICE POLICE PURSUIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21702·2020-10-15

    Peloton Recalls PR70P Bike Pedals Due to Laceration Hazard

    Peloton is recalling PR70P clip-in pedals fitted on bikes sold between July 2013 and May 2016 because they can break unexpectedly, causing laceration injuries.

    Product
    PR70P Clip-In Pedals fitted on Peloton bikes (sold between July 2013 and May 2016)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V637000·2020-10-15

    Genie Recalls 2020 TZ-34 and TZ-50 Trailer-Mounted Boom Lifts

    Genie is recalling 2020 TZ-34 and TZ-50 trailer-mounted boom lifts because under-tightened bolts may affect stability and increase injury risk.

    Product
    GENIE — GENIE TZ-50, TZ-34
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21703·2020-10-15

    Homerygardens Extension Cord Splitters Recalled for Fire Hazard

    Sales BSD is recalling Homerygardens extension cord splitters because the wire size cannot handle the appropriate amp load, posing a fire hazard.

    Product
    Homerygardens™ 4-Outlet, 6-Foot Long Indoor and Outdoor Extension Cord Splitters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0082-2021·2020-10-14

    Biomet OnPoint Scope Procedure Kit Recalled for Sterilization Defect

    Biomet is recalling OnPoint Scope Procedure Kits because they were not properly aligned with the gamma sterilization group, resulting in improper sterilization.

    Product
    Biomet OnPoint SCOPE PROCEDURE KIT Item Number: 24-3050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0085-2021·2020-10-14

    Roche BenchMark ULTRA Advanced Staining System Recalled for Electrical Fire Risk

    Roche Diagnostics is recalling BenchMark ULTRA Advanced Staining Systems due to a risk of fluid leaks causing electrical shorts, heat, and fire.

    Product
    BenchMark ULTRA Advanced Staining System (IVD)- Material Number: 05342716001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V631000·2020-10-14

    Mercedes-Benz Recalls 2020 Sprinter Vans Due to Brake Hose Defect

    Daimler Vans USA is recalling 2020 Mercedes-Benz Sprinter vans because damaged brake hoses may leak fluid, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0086-2021·2020-10-14

    Roche Discovery Ultra Staining System Recalled for Electrical Short Risk

    Roche Diagnostics is recalling the DISCOVERY ULTRA Advanced Staining System due to fluid leaks that can cause electrical shorts, heat, and smoke.

    Product
    DISCOVERY ULTRA Advanced Staining System (RUO-Research Use Only) Material Number: 05987750001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0059-2021·2020-10-14

    AB ULAX 1500 Flex Heat and Moisture Exchanger Recall for Disconnection Risk

    AB ULAX is recalling 1500 Flex Heat and Moisture Exchangers because they may disconnect from the respiratory circuit, potentially causing hypoxia or death.

    Product
    1500 Flex Heat and Moisture Exchanger, Catalog Reference 150 - Product Usage: Heat Moisture Exchangers (HM Es) are designed to enhance humification of ventilator-dependent and non-ventilator dependent patients in critical care, home care and anesthesia.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0081-2021·2020-10-14

    Biomet Regenerex Primary Taper Cap Recalled for Sterilization Defect

    Biomet is recalling Regenerex Primary Taper Caps because they were not properly aligned for gamma sterilization, potentially leaving them unsterilized.

    Product
    Biomet Regenerex Primary Taper Cap Item Number 141269
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V633000·2020-10-14

    Toyota Recalls 2020 Highlanders Due to Seat Airbag Deployment Risk

    Toyota is recalling 2020 Highlander and Highlander Hybrid vehicles because incorrect seat trim covers may prevent side airbags from deploying properly, increasing injury risk in a crash.

    Product
    TOYOTA — TOYOTA HIGHLANDER, HIGHLANDER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0060-2021·2020-10-14

    DJO EMPOWR Tibial Knee Punch Handle Recall Due to Retaining Pin Risk

    Encore Medical is recalling 190 units of DJO EMPOWR Tibial Knee Punch Handles because the retaining pin may fall out, potentially leaving debris in the joint space.

    Product
    DJO EMPOWR Tibial Knee Punch Handle Part No. 801-05-040 and 801-05-018 contained in Instrument Tray for EMPOWR Porous Knee - Product Usage: The Tibial Punch Handle is used in conjunction with one of three appropriately sized Tibial Punch Guides to broach the tibial canal in…
    Category
    Medical Device
    Distribution
    Distributed nationwide