The Recall Desk

State

US Virgin Islands product recalls

73,827 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.

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.

57676–57700 of 74005

  • LowFDA (Devices)·Z-2127-2014·2014-08-06

    Small Bone Innovations Recalls AutoFIX Cannulated Compression Screw Systems for IFU Update

    Small Bone Innovations is recalling 506 units of 3.0/4.0mm AutoFIX Cannulated Compression Screw Systems to update the Instructions for Use (IFU).

    Product
    Small Bone Innovations 3.0/4.0mm AutoFIX" Cannulated Compression Screw System Sets, Implants, and Instruments Indications for Use: AutoFIX" cannu lated screws are indicated for the treatment of fractures, non-unions, pseudoarthrosis and degenerative changes as well as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14250·2014-08-05

    Samson International Recalls Spencer Bar Stool Due to Fall Hazard

    Samson International is recalling Spencer Bar Stools sold at Costco because the footrest can crack, posing a fall hazard. No injuries have been reported.

    Product
    Spencer Bar Stool
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14249·2014-08-05

    Scubapro Aladin2 Dive Computers Recalled for Decompression Sickness Risk

    Johnson Outdoors Diving is recalling Scubapro Aladin2 dive computers because they may leak and stop working, posing a risk of injury from decompression sickness.

    Product
    Scubapro Aladin2 dive computers, commonly referred to as Aladin Square dive computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V476000·2014-08-04

    Grand Design Recalls 2014 Momentum Trailers Due to Suspension Bolt Defect

    Grand Design is recalling 2014 Momentum 355th, 380th, and 385th fifth wheel trailers because suspension bolts may shear, potentially causing a crash.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM 385TH, MOMENTUM 380TH, MOMENTUM 355TH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V475000·2014-08-04

    Toyota Recalls FJ Cruiser and Tacoma for Incorrect Tire Placard Information

    Toyota is recalling 2008-2014 FJ Cruiser and Tacoma vehicles with specific accessory wheels because the tire placard may list incorrect spare tire size or inflation pressure.

    Product
    TOYOTA — TOYOTA FJ CRUISER, TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V473000·2014-08-01

    Nova Bus Recalls 2013 LFS Transit Buses for Wiper Linkage Bolt Issue

    Nova Bus is recalling 189 model year 2013 LFS transit buses because a windshield wiper linkage bolt may loosen, potentially rendering wipers inoperable and increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V467000·2014-07-31

    Jayco Recalls 2013-2014 Seneca Motorhomes Due to Fire Risk

    Jayco is recalling 2013-2014 Seneca motorhomes because water infiltration into the entrance door keypad may cause corrosion and an electrical short, increasing the risk of a fire.

    Product
    JAYCO — JAYCO SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V469000·2014-07-31

    Schwarze M6000SE CNG Street Sweepers Recalled for Fire Risk

    Schwarze is recalling 2009 M6000SE CNG street sweepers because condensation in the intake manifold may freeze, causing sensor failure and potential exhaust fires.

    Product
    SCHWARZE — SCHWARZE M6000SE CNG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14245·2014-07-31

    Dynacraft Recalls Avigo Youth Bicycles Due to Front Wheel Detachment Hazard

    Dynacraft is recalling Avigo 20-inch youth bicycles because the front wheel can detach, posing a fall hazard. One injury involving scrapes and abrasions has been reported.

    Product
    Avigo 20-inch Turn N' Burn Youth Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V468000·2014-07-31

    Jayco Recalls 2014-2015 White Hawk Travel Trailers Due to Tire Wear

    Jayco is recalling 2014-2015 White Hawk Summit 27RBOK travel trailers because a tire may rub against the outrigger, causing premature wear or failure.

    Product
    JAYCO — JAYCO, JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V466000·2014-07-31

    Entegra Recalls 2014-2015 Cornerstone Motorhomes for Seat Belt Defect

    Entegra is recalling 2014-2015 Cornerstone motorhomes because incorrect seat belt attachments may cause fraying and reduced strength, increasing injury risk in crashes.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2068-2014·2014-07-30

    GE Healthcare Recalls DateX-Ohmeda S/5 Airway Modules Due to CO2 Measurement Failure

    GE Healthcare is recalling DateX-Ohmeda S/5 Single-Width Airway Modules and E-miniC accessories because a CO2 detector failure may cause incorrect low readings, potentially impairing clinical decision-making for ventilated patients.

    Product
    DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE, E-MINIC AND ACCESSORIES. DATEX-OHMEDA S/5TM FM WITH L-FICU04 ANDL-FICUO4A SOFTWARE AND N-FCREC MODULE **(OUS only). E-miniC and accessories is indicated for monitoring C02 and respiration rate of all hospital patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2080-2014·2014-07-30

    Stryker Recalls Disposable StrykeFlow Tips Due to Sterility Concerns

    Stryker Endoscopy is recalling 496 boxes of Disposable StrykeFlow Tips because a deformed blister pouch could compromise the product's sterility.

    Product
    Disposable StrykeFlow Tip, Stryker Disposable Suction/I irrigator Tip; Sterile, Rx only, Latex Free. Stryker Suction Irrigation system, used to provide a clean and clear operative site through the evacuation and aspiration of irrigant solution. for endoscopic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V463000·2014-07-30

    Utility Trailer Recall for Potential Pintle Hook Safety Chain Failure

    Utility Trailer Manufacturing Company is recalling certain 2012-2014 utility trailers because the pintle hook safety chain loop may break, increasing crash risk.

    Product
    UTILITY — UTILITY, UTILITY TRAILER VS1RA, VS2DX, VS2RA, VS3DX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2021-2014·2014-07-30

    Blood Glucose Test Strips Recalled for Inappropriate Labeling and Marketing

    Diabetic Supply of Suncoast, Inc. is recalling Advocate Redi-Code+ blood glucose test strips because they were inappropriately labeled and marketed.

    Product
    ADVOCATE Redi-Code+ BMB-BA006A Blood Glucose test strips Product Usage: The ADVOCATE¿ Redi-Code+ BMB-BA006A Blood Glucose test strips are used only with the ADVOCATE¿ Redi-Code+ BMB-EA004S meter to quantitatively measure glucose in fresh capillary whole blood samples drawn…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V464000·2014-07-30

    Suzuki Recalls 2010-2013 Kizashi Vehicles for Fuel Tank Fire Risk

    Suzuki is recalling 2010-2013 Kizashi vehicles because spider webs may block a fuel system hose, causing a fuel leak and increasing the risk of a fire.

    Product
    SUZUKI — SUZUKI KIZASHI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2116-2014·2014-07-30

    Pentax Ultrasound Gastroscopes Recalled Due to Aspiration Needle Derailment Risk

    Pentax Medical is recalling 531 ultrasound gastroscopes because aspiration needles may derail from the accessory elevator, posing a risk of patient injury.

    Product
    EG-3630U Ultrasound Video Gastroscope EG-3830UT Ultrasound Video Gastroscope EG-3870UTK Ultrasound Video Gastroscope FG-36UX Ultrasound Fiber Gastroscope Used to provide optical and sonographic visualization of and therapeutic access to the Upper Gastrointestinal Tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2198-2014·2014-07-30

    Metagenics Recalls UltraBalance Protein Powder for Undeclared Soy

    Metagenics is recalling UltraBalance Protein Powder because it may contain undeclared soy. The recall covers specific lots distributed nationwide and internationally.

    Product
    UltraBalance Protein Powder, Net Wt. 14.8 oz (420g)
    Category
    Food
    Distribution
    Distributed nationwide