The Recall Desk

State

US Virgin Islands product recalls

73,597 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 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29201–29225 of 73775

  • ModerateFDA (Devices)·Z-1739-2020·2020-04-29

    Boston Scientific Recalls Stretch VL Ureteral Stent Sets Due to Tracking Issues

    Boston Scientific is recalling 40 units of Stretch VL Ureteral Stent Sets because they may be difficult to track over a guidewire, potentially delaying procedures.

    Product
    Stretch VL Ureteral Stent Set 7FX22-30CM with .035 Sensor UPN: M006185157080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V236000·2020-04-28

    Triumph Recalls Motorcycles Due to Front Brake Pad Corrosion Risk

    Triumph is recalling 3,709 motorcycles because front brake pads may corrode and detach, increasing stopping distance and crash risk.

    Product
    TRIUMPH — TRIUMPH XRX (LRH), STREET TRIPLE RS, SPEED TRIPLE RS, SPEED TRIPLE S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V238000·2020-04-28

    Jayco Recalls 2020 Jay Flight SLX Trailers Due to Propane Leak Risk

    Jayco is recalling 2020 Jay Flight SLX travel trailers because an improperly tightened propane hose may leak, increasing the risk of fire or explosion.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V237000·2020-04-28

    Forest River Recalls 2020 StarTrans PS2 Buses for Seat Belt Defect

    Forest River is recalling 2020 StarTrans PS2 transit buses because seat belt retractors may not secure occupants properly, increasing injury risk in crashes.

    Product
    STARTRANS — STARTRANS PS2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V233000·2020-04-27

    MCI J4500 and J3500 Motor Coaches Recalled for Brake Hose Defect

    Motor Coach Industries is recalling 2014-2019 J4500 and 2018-2019 J3500 motor coaches because brake hoses may crack, causing air leaks and increased stopping distances.

    Product
    MCI — MCI J4500, J3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V234000·2020-04-27

    Blue Bird Recalls School Buses for Parking Brake Defect

    Blue Bird is recalling 2006-2021 Vision and 2007-2013 All American school buses because the parking brake may fail to hold the vehicle on an incline.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V235000·2020-04-27

    Blue Bird Recalls 2009-2019 Vision Buses for Parking Brake Defect

    Blue Bird is recalling 2009-2019 Vision transit buses because the floor-mounted parking brake may fail to hold the vehicle on an incline when fully loaded.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E026000·2020-04-24

    Denso Fuel Pump Recall for Potential Engine Stall Risk

    Denso is recalling certain fuel pumps where an impeller may crack and deform. This defect can cause the engine to stall while driving, increasing the risk of a crash.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E025000·2020-04-24

    Ford Recalls Replacement Headlamps for 2013-2016 Lincoln MKZ Vehicles

    Ford is recalling specific replacement headlamps for 2013-2016 Lincoln MKZ vehicles because they may have improper beam patterns and missing markings, potentially reducing visibility.

    Product
    LINCOLN — LINCOLN MKZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20112·2020-04-23

    Leviton Recalls 50-Ampere Electrical Connectors Due to Shock Hazard

    Leviton is recalling approximately 98,000 50-ampere electrical connectors, plugs, receptacles, and inlets sold in the US and Canada due to mislabeled terminal markings that pose an electrical shock hazard.

    Product
    Leviton 50 ampere, non-NEMA electrical connectors, plugs, receptacles and inlets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V231000·2020-04-23

    McLaren Recalls 2,763 Vehicles for Fuel Tank Corrosion Risk

    McLaren is recalling 2,763 vehicles because a foam pad may corrode the fuel tank, potentially causing a leak and fire risk.

    Product
    MCLAREN — MCLAREN 570 GT, SENNA, 720S, GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20738·2020-04-23

    LUS Recalls Hair Dryers Due to Electrocution or Shock Hazard

    LUS Distribution Inc. is recalling approximately 2,700 hair dryers and diffusers sold in the U.S. because they lack immersion protection, posing an electrocution or shock hazard if they fall into water.

    Product
    LUS Hair Dryers & Diffusers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0892-2020·2020-04-22

    Mountain Rose Herbs Recalls Kudzu Root Due to Salmonella Risk

    Mountain Rose Herbs is recalling specific lots of Kudzu Root because they may be contaminated with Salmonella. The product was sold nationwide in the US and in Canada.

    Product
    Kudzu Root (Pueraria montana var. lobata), This product was packaged in a clear plastic bag or poly-woven bags sold in bulk form net weight ranges from 4 ounces to 20 pounds. The label is read in parts: "***Kudzu Root***Herbal Supplement **Origin: China** MOUNTAIN ROSE HERBS…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1238-2020·2020-04-22

    Losartan Potassium Tablets Recalled Due to NBMA Impurity Detection

    Golden State Medical Supply Inc. is recalling Losartan Potassium Tablets 25 mg because an impurity, NBMA, was detected in the active ingredient.

    Product
    Losartan Potassium Tablets, USP, 25 mg, Rx only, a) 30 ct. (NDC 60429-316-30) b) 90ct. (NDC 60429-316-90) c) 1,000 ct. (60429-316-10) bottles, GSMS Incorporated, Manufactured by Arrow Pharm (Malta) Ltd., Packaged by GSMS Incorporated, Camarillo, CA 93012, USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V230000·2020-04-22

    Lode King Prestige Semi-Trailers Recalled for Cargo Winch Mount Defect

    Lode-King is recalling 2015-2021 Prestige SDG53-2 step-deck semi-trailers because cargo winch mounts may fail, allowing cargo to fall off and create road hazards.

    Product
    LODE KING — LODE KING PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1703-2020·2020-04-22

    Sysmex CF-70 Blood Smear Transporter Recalled for Software Mismatch Hazard

    Sysmex America is recalling 93 CF-70 instruments because a software mismatch may prevent the device from halting when the cover door is opened.

    Product
    The CF-70 instrument (product code: LXG; Regulation Number: 862.2050) receives magazines containing stained blood smears from SP-50, selects only smears that require analysis, and transports them to the DI-60 for further analysis. After completing the analysis on DI-60 the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1699-2020·2020-04-22

    Stago STA-Deficient VIII Plasma Recalled for Cross-Contamination Risk

    Diagnostica Stago is recalling STA-Deficient VIII plasma due to a risk of sample-to-sample cross-contamination that may cause falsely increased factor VIII levels.

    Product
    STA - Deficient VIII, Product Code: 00725. STA - Deficient VIII is an immuno-depleted human plasma intended for use in tests for the determination of factor VIII activity in plasma on STA-R and STA Compact analyzer platforms as follows: (A) STA-R Max, Product Codes: 58989…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V226000·2020-04-22

    Mercedes-Benz Recalls 2020 GLE Models Due to Air Bag Wiring Defect

    Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because a pinched wiring harness may prevent rear side air bags from deploying correctly.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1698-2020·2020-04-22

    Boston Scientific Recalls Nitinol Thermocouple Electrodes Due to Incorrect Instructions

    Boston Scientific is voluntarily correcting 43 units of Nitinol Thermocouple Electrodes because they were packaged with incorrect Instructions for Use.

    Product
    Nitinol Thermocouple Electrode, 5cm - Product Usage: The TCN Electrode is indicated for use in RF heat lesioning of peripheral nerve tissue only.The Cosman Medical TCN Electrodes are temperature-sensing probes for use in the percutaneous treatment of pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide