The Recall Desk

State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58901–58925 of 74011

  • SevereNHTSA·14V183000·2014-04-07

    Oshkosh Recalls S-Series Trucks Due to Exhaust Fire Risk

    Oshkosh is recalling 2012-2014 S-Series Ready Mixed Concrete trucks because condensation in the intake manifold may freeze, causing elevated exhaust temperatures or flames that increase the risk of fire or burn injury.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V172000·2014-04-04

    MCI E4500 and J4500 Motorcoaches Recalled for Seat Track Weld Defect

    Motor Coach Industries is recalling 2009-2014 E4500 and J4500 motorcoaches because a missing weld on second-row seat tracks could cause seats to detach in a crash.

    Product
    MCI — MCI E4500, J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14144·2014-04-04

    Hussong Recalls Gas Fireplaces and Inserts Due to Explosion Hazard

    Hussong Manufacturing is recalling about 13,600 gas fireplaces and inserts in the U.S. because a control module defect can cause gas buildup and explosions.

    Product
    Kozy Heat, Ambiance and Stellar Hearth gas fireplaces and fireplace inserts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V238000·2014-04-03

    Navistar Recalls 2014 International TranStar Trucks Due to Fire Risk

    Navistar is recalling 2014 International TranStar trucks with specific Cummins engines because condensation may freeze and cause exhaust flames or fire.

    Product
    INTERNATIONAL — INTERNATIONAL TRANSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V173000·2014-04-03

    Mazda Recalls 2014-2015 Models for Potential Engine Stall Risk

    Mazda is recalling 2014-2015 Mazda3 and Mazda6 vehicles because a software error may cause the engine to stall in heavy rain, increasing crash risk.

    Product
    MAZDA — MAZDA MAZDA6, MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V170000·2014-04-03

    Mazda Recalls 2014 Mazda6 Vehicles for Fuel Tank Overfill Risk

    Mazda is recalling approximately 19,000 2014 Mazda6 vehicles because the fuel tank can be overfilled, potentially causing gas to leak and increasing fire risk.

    Product
    MAZDA — MAZDA MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14C003000·2014-04-03

    Evenflo Recalls Child Seats With Stuck Harness Buckles

    Evenflo is recalling specific convertible and harnessed child seats because the harness buckle may become stuck, making it difficult to remove a child in an emergency.

    Product
    CHILD SEAT:HARNESS/CROTCH BUCKLE recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14727·2014-04-03

    K2 Kwicker Snowboard Bindings Recalled for Unexpected Release Hazard

    K2 Sports is recalling Kwicker and Kwicker BC snowboard bindings because they can release unexpectedly, posing a fall hazard to users.

    Product
    K2 Kwicker and Kwicker BC snowboard bindings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1227-2014·2014-04-02

    Thoratec HeartMate II Implant Kit Recalled Due to Controller Switching Injuries

    Thoratec is recalling HeartMate II Implant Kits because serious injuries and deaths occurred when patients switched from primary to backup System controllers.

    Product
    HeartMate II Implant Kit with Pocket Controller; with sealed grafts (NAm) with sealed grafts (EU) Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately on its own.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1230-2014·2014-04-02

    Thoratec HeartMate II Pocket Controllers Recalled Due to Reported Deaths

    Thoratec is recalling HeartMate II Pocket Controllers because serious injuries and deaths were reported when patients switched from primary to backup controllers.

    Product
    Heart Mate II Pocket Controllers removed from packaging Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately on its own.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1228-2014·2014-04-02

    Thoratec HeartMate II System Controller Recalled Due to Injury and Death Reports

    Thoratec is recalling HeartMate II System Controllers because serious injuries and deaths occurred when patients switched from primary to backup controllers.

    Product
    HeartMate II System Controller Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately on its own. It is sometimes called a a heart pump or VAD. HeartMate II is a small implantable LVAD.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-229-2014·2014-04-02

    Thoratec HeartMate II LVAD Pump Recall Due to Controller Switching Injuries

    Thoratec is recalling 36 HeartMate II LVAD Pump and Pocket Controller Kits because switching from the primary to the backup controller caused serious injuries and deaths.

    Product
    HeartMate II LVAD Pump and Pock Controller Kit; Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately on its own.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1301-2014·2014-04-02

    BioCardia Morph AccessPro Steerable Introducer Recalled for Particulate Risk

    BioCardia is recalling Morph AccessPro Steerable Introducers due to potential particulates in the inner lumen that could cause an embolic event.

    Product
    Morph AccessPro Steerable Introducer; 6F Introducer, 45 cm working length Single use only. BioCardia, Inc. San Carlos, CA 94070 BioCardia Morph AccessPro is intended to provide a pathway through medical instruments cush as balloon dilation catheters, guidewires or other…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1272-2014·2014-04-02

    Siemens AXIOM Artis Systems Recalled for Potential Gantry Drop Risk

    Siemens is recalling 37 AXIOM Artis angiography systems because a cooling unit defect may cause a system failure and gantry drop.

    Product
    AXIOM Artis Systems Product usage: Artis zee is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1275-2014·2014-04-02

    Velocity Medical Solutions Recalls DICOM Export Format Software

    Velocity Medical Solutions is recalling DICOM Export Format for Sum Dose v3.0.0 software because it may replace calculated doses in Eclipse treatment plans.

    Product
    DICOM Export Format for Sum Dose with Velocity v3.0.0. A stand-alone software product that provides the oncology care specialists (physicians, physicists, dosimetrists, etc.) a means for comparison of medical imaging data from multiple DICOM conformant imaging modality…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V164000·2014-04-02

    Ford Recalls 2013-2014 Vehicles Due to Weak Seatback Welds

    Ford is recalling 2013-2014 Fusion, Escape, C-Max, and Lincoln MKZ vehicles because sub-standard welds may cause seatbacks to loosen, increasing injury risk in crashes.

    Product
    FORD — FORD, LINCOLN ESCAPE, MKZ, C-MAX, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·020-2014·2014-04-02

    Backpackers Pantry Recalls Fettuccini Alfredo With Chicken Due to Undeclared Allergens

    American Outdoor Products is recalling 633 pounds of dehydrated Fettuccini Alfredo with Chicken because the packaging contains undeclared milk and wheat allergens.

    Product
    American Outdoor Products, Inc — Colorado Firm Recalls Fettuccini Alfredo With Chicken Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1278-2014·2014-04-02

    Teleflex Recalls Weck Vista Optical Bladeless Laparoscopic Access Ports

    Teleflex Medical is recalling 55,521 Weck Vista Optical Bladeless Laparoscopic Access Ports due to reported gas leakage that may delay surgical procedures.

    Product
    5/10 mm Weck¿, Vista" Optical Bladeless Laparoscopic Access Port, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1293-2014·2014-04-02

    Teleflex Medical Recalls Polypropylene Sutures for Needle Attachment Defect

    Teleflex Medical is recalling non-absorbable polypropylene sutures because they failed to meet minimum needle attachment strength requirements.

    Product
    Sutures, Non-absorbable, Synthetic, Polypropylene, Sterile, Rx only, Product Usage: Non-absorbable polypropylene surgical suture is a monofilament, Non-absorbable, sterile, flexible thread prepared from long-chain polyolefin polymer known as polypropylene and is indicated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1284-2014·2014-04-02

    Teleflex Medical Recalls Weck Vista Universal Cannula Due to Gas Leakage

    Teleflex Medical is recalling 55,521 units of Weck Vista Universal Cannulas because they may leak insufflation gas, potentially delaying laparoscopic surgeries.

    Product
    5/10/12 mm Weck¿ Vista" Universal Cannula, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14E009000·2014-04-02

    Villa Recalls Motorhome Seats Due to Seat Belt Fraying Risk

    Villa International is recalling specific driver and passenger seats used in 2013-2014 Tiffin and American Coach motorhomes because the seat belts may fray and fail to restrain occupants.

    Product
    TIFFIN — TIFFIN, AMERICAN COACH ALLEGRO BUS, AMERICAN TRADITION, EAGLE, AMERICAN REVOLUTION
    Category
    Vehicle
    Distribution
    Distributed nationwide