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.

61326–61350 of 74011

  • HighNHTSA·13V540000·2013-10-28

    Forest River Recalls Travel Trailers with Incorrect Tire Pressure Labels

    Forest River is recalling 2008-2011 travel trailers because incorrect tire inflation pressures on the certification label may lead to overinflation and sudden tire failure.

    Product
    FLAGSTAFF — FLAGSTAFF, ROCKWOOD, CHEROKEE TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V531000·2013-10-25

    Spartan Motor Home Recall for Potential Steering Linkage Separation

    Spartan is recalling 175 model year 2013-2014 motor homes and one chassis because loose steering linkage fasteners may cause a loss of steering.

    Product
    SPARTAN — SPARTAN METROSTAR, K3, K2, MM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V526000·2013-10-25

    BMW Recalls 2012 K 1600 GT Motorcycles for Throttle Software Issue

    BMW is recalling 2,475 model year 2012 K 1600 GT and GTL motorcycles because a software error may cause the engine to stall, increasing crash risk.

    Product
    BMW — BMW K 1600 GT, K 1600 GTL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14005·2013-10-24

    Emerson Recalls Tommy Bahama Outdoor Ceiling Fans Due to Injury Risk

    Emerson Air Comfort Products is recalling specific Tommy Bahama outdoor ceiling fans because brackets can break, causing blades to fall and injure bystanders.

    Product
    Tommy Bahama® Outdoor Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0010-2014·2013-10-23

    GE Healthcare Recalls Ventilators and Anesthesia Machines with Unresponsive Buttons

    GE Healthcare is recalling 911 ventilators and anesthesia machines because manufacturing defects may cause display buttons to fail, preventing access to menu functions.

    Product
    GE Healthcare, Avance, Avance CS2, Aisys, Aespire View, and Engstrom. Intended for volume or pressure control ventilation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0009-2014·2013-10-23

    GE Healthcare Recalls Anesthesia Devices Due to Tidal Volume Overdelivery Risk

    GE Healthcare is recalling specific anesthesia devices because they may deliver excessive tidal volume in a specific ventilation mode, posing a risk of harm to patients.

    Product
    GE Healthcare, Aisys, Amingo, Avance, and Avance CS2. Intended for volume or pressure control ventilation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0005-2014·2013-10-23

    Dutch Valley Mixed Nuts Recalled for Undeclared Pecans

    Dutch Valley Food Development Inc. is recalling Roasted Salted Mixed Nuts with Peanuts due to undeclared pecans in the ingredient statement.

    Product
    Roasted Salted Mixed Nuts w/ Peanuts, net wt. 12 oz., packed in a clear plastic bag. Ingredients: blanched peanuts, unblanched peanuts, unblanched almonds, unblanched Brazil nuts, unblanched filberts, cashews cooked in canola oil, salt. Allergen info: peanut and tree…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0024-2014·2013-10-23

    GE PET Discovery 610 and 710 Recalled for Image Series UID Conflict

    GE Healthcare is recalling PET scanners because a software issue may cause different image series to share the same ID, potentially leading to incorrect image display.

    Product
    GE PET Discovery 610, PET Discovery 710. Intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0025-2014·2013-10-23

    Boston Scientific COGNIS CRT-D Recall for Premature Battery Depletion

    Boston Scientific is recalling COGNIS CRT-D devices because a capacitor defect may cause premature battery depletion.

    Product
    Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. The following models are not available in the US: models N106, N107, P106, P107. Sterilized using ethylene oxide. Boston Scientific, 4100 Hamline Avenue North, St. Paul, MN…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0026-2014·2013-10-23

    Boston Scientific TELIGEN ICDs Recalled for Premature Battery Depletion Risk

    Boston Scientific is recalling TELIGEN implantable cardiac defibrillators because a capacitor defect may cause premature battery depletion.

    Product
    Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models are not available in the US: models F102, F110, F111. Sterilized using ethylene oxide. Boston Scientific, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA. Indicated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0011-2014·2013-10-23

    Siemens Recalls ADVIA Hematology Systems Due to Sample Labeling Error Risk

    Siemens is recalling ADVIA 2120/2120i hematology systems connected to an ADVIA Autoslide because a rack jam error could cause the next slide to be labeled with the wrong sample identification information.

    Product
    ADVIA 2120/2120i Hematology Systems with ADVIA Autoslide connected to it, SMN 10361162 and SMN 10361798 --- CLASSIFICATION NAME: Counter, Differential Cell, Automated (Particle Counter) The ADVIA 2120/2120i are hematology systems that utilizes the principles of flow cytometry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-66272-001·2013-10-23

    Infant ibuprofen drops are recalled nationwide for process-related particulates

    McNeil Consumer Healthcare is recalling 197,532 bottles of Concentrated Motrin Infants' Drops because process-related particulates were observed. The affected bottles were distributed nationwide.

    Product
    Concentrated Motrin (ibuprofen) Infants' Drops Oral Suspension, Original Berry Flavor 1/2 fl oz bottles, 50 mg per 1.25ml, Distributed by McNeil Consumer Healthcare, Fort Washington, PA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0014-2014·2013-10-23

    Synthes Midfoot Fusion Bolt Recall for Technique Guide Clarification

    Synthes USA is recalling 62 Midfoot Fusion Bolts to update the technique guide, emphasizing supplemental fixation to reduce the risk of bolt back-out or migration.

    Product
    Synthes Midfoot Fusion Bolt 6.5 mm. It is indicated for fracture, fixation, osteotomies, nonunions, and fusions of large bones in the foot and ankle.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0018-2014·2013-10-23

    Getinge 46-Series Washer-Disinfectors Recalled for Overheating Risk

    Getinge Disinfection is recalling 46-Series medical washer-disinfectors due to a possible overheating hazard. The voluntary field safety correction affects 143 units distributed in the US and Canada.

    Product
    Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The washer disinfector is used in healthcare facilities where reusable items such as instruments, utensils, anesthesia sets, and glassware are handled for decontamination purposes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V563000·2013-10-23

    Exiss and Sooner Travel Trailer Door Lock Recall

    NHTSA is recalling 2006-2013 Exiss and Sooner travel trailers because a door lock defect may jam the deadbolt, trapping occupants inside.

    Product
    SOONER — SOONER, EXISS TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0012-2014·2013-10-23

    GE Healthcare X-ray Systems Recalled for Loose Power Assist Handle Bolts

    GE Healthcare is recalling 810 X-ray systems because internal bolts on the power assist handle may loosen or fall out, potentially causing the handle to stick in the ON position.

    Product
    GE Healthcare, Precision 500D, Legacy, RFX, and SFX X. This table is intended for use in a diagnostic X-ray system to support patients during general purpose radiological procedures in the horizontal, vertical and trendelenburg positions. - The Expedio 500D is designed to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0022-2014·2013-10-23

    Harvest Graft Delivery System Recalled for Potential Luer Connector Leaks

    Harvest Technologies is recalling 730 cases of the Harvest Graft Delivery System because the Luer connector may leak or crack.

    Product
    Harvest Graft Delivery System; Model Number: GDP-10 Product Usage: The Harvest Graft Delivery System is intended for the aspiration of bone marrow, autologous blood, plasma, or other body fluids. The system is indicated for die delivery of allograft, autograft, or synthetic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13C003000·2013-10-23

    Orbit Baby Recalls G2 Car Seat Bases Due to Knob Defect

    Orbit Baby is recalling specific G2 Car Seat Bases because the StrongArm Knob may detach or spin, potentially failing to secure the base in a crash.

    Product
    CHILD SEAT:BASE recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0004-2014·2013-10-23

    Dutch Valley Honey Roasted Peanuts Recalled for Undeclared Allergens

    Dutch Valley Food Development Inc. is recalling Honey Roasted Peanuts due to undeclared milk and wheat allergens.

    Product
    Honey Roasted Peanuts, net wt. 11 oz.., packed in a clear plastic bag. Ingredients: peanuts, sugar, peanut and/or canola and/or cottonseed oil, honey, salt, modified potato starch, xanthan gum. Allergen info: peanut and soy ingredients. Also states that facility also…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·13V533000·2013-10-23

    Trailex Recalls Enclosed Car Trailers Due to Door Lock Jamming Risk

    Trailex is recalling certain enclosed car trailers because a defect in the door locks may jam the deadbolt, potentially trapping occupants inside.

    Product
    TRAILEX — TRAILEX CTE-80180, CTE-80210 HD, CTE-84180
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0015-2014·2013-10-23

    OSOM C. Difficile Toxin A/B Test Kit Recalled for False Negative Risk

    Sekisui Diagnostics is recalling specific lots of the OSOM C. Difficile Toxin A/B Test Kit due to the potential for false negative results.

    Product
    Product Name: OSOM C. Difficile Toxin A/B Test Catalog Numbers: 173 (for United States) and 173 E (for Europe). The Test is a qualitative assay (in vitro diagnostic) that employs immunochromatographic, dipstick technology. If C. difficile toxin A or toxin B is present, a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V499000·2013-10-23

    Neo Trailers Recalls 2010-2011 Models Due to Door Lock Jamming Risk

    Neo Manufacturing is recalling 2010-2011 cargo trailers because a defect in Fastec door locks may jam the deadbolt, potentially trapping occupants inside.

    Product
    NEO TRAILERS — NEO TRAILERS NAV, NCV, NAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0021-2014·2013-10-23

    GE Healthcare Recalls X-ray Systems Due to Missing Monitor Screws

    GE Healthcare is recalling specific X-ray imaging systems because missing screws in the overhead video monitor suspension could create a safety hazard.

    Product
    GE Healthcare, Advantx, Innova 2000, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ. Intended for general purpose diagnostic fluoroscopy and radiography studies.
    Category
    Medical Device
    Distribution
    Distributed nationwide