The Recall Desk

State

US Virgin Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44301–44325 of 73984

  • HighNHTSA·17V162000·2017-03-13

    Thor Motor Coach Recalls 2014-2016 Motorhomes for Wiper Defect

    Thor Motor Coach is recalling specific 2014-2016 motorhomes because improperly installed windshield wipers may fail, impairing visibility and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MOTOR DAYBREAK, ACE, CHALLENGER, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V165000·2017-03-13

    Ride The Ducks Recalls Amphibious Vehicles for Instrument Cluster Defect

    Ride The Ducks International LLC is recalling 1996-2014 amphibious vehicles because the instrument cluster fails to properly illuminate turn signal and high beam indicators, potentially increasing crash risk.

    Product
    RIDE THE DUCKS — RIDE THE DUCKS AMPHIBIOUS VEHICLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V166000·2017-03-13

    Thor Motor Coach Recalls 2017 Motorhomes Due to Missing Seat Belts

    Thor Motor Coach is recalling 2017 Chateau, Freedom Elite, and Four Winds motorhomes because the middle sofa seat may lack a seat belt, increasing crash injury risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FREEDOM ELITE, FOUR WINDS, CHATEAU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V158000·2017-03-10

    Polaris Recalls 2017 Slingshot Models for Steering Bolt Tightening Defect

    Polaris is recalling 2017 Slingshot, SL, and SLR vehicles because three steering and suspension bolts may be insufficiently tightened, potentially reducing vehicle handling.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V159000·2017-03-10

    Kia Recalls 2017 Niro Hybrid for Power Steering Connector Defect

    Kia is recalling 2017 Niro Hybrid vehicles because a damaged steering connector may cause a loss of power steering assist, increasing the risk of a crash.

    Product
    KIA — KIA NIRO HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17108·2017-03-10

    R.W. Beckett Recalls Firomatic Fuel Oil Valves Due to Fire Hazard

    R.W. Beckett is recalling approximately 18,000 Firomatic fusible safety valves because the stem may fail to seal, allowing fuel to leak and posing a fire hazard.

    Product
    Firomatic® fusible safety valves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V154000·2017-03-09

    Land Rover Recalls 2016 Range Rovers for Passenger Air Bag Defect

    Jaguar Land Rover is recalling 2016 Range Rover and Range Rover Sport vehicles because the passenger air bag inflator may fail to ignite, preventing deployment in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·023-2017·2017-03-09

    King's Command Foods Recalls Beef Products Due to Foreign Matter

    King's Command Foods is recalling approximately 26,138 pounds of ground beef products due to possible contamination with extraneous materials, including metal objects.

    Product
    King's Command Foods, LLC — King's Command Foods, LLC. Recalls Beef Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V153000·2017-03-09

    Jaguar Recalls 2017 F-PACE Vehicles Due to Short Rear Driveshaft

    Jaguar is recalling 2017 F-PACE vehicles with automatic transmissions because a short rear driveshaft may separate, causing loss of drive power and increasing crash risk.

    Product
    JAGUAR — JAGUAR F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V155000·2017-03-09

    Airstream Recalls 2017 Base Camp Trailers Due to Tire Contact Risk

    Airstream is recalling 2017 Base Camp recreational trailers because heavy loads may cause tires to contact the wheel well liner, risking tire failure and crashes.

    Product
    AIRSTREAM — AIRSTREAM BASECAMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V156000·2017-03-09

    Gillig Recalls 2016-2017 Low Floor Buses for Wiper Arm Defect

    Gillig is recalling 2,732 Low Floor transit buses because wiper arms can crack and detach, reducing driver visibility and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17107·2017-03-09

    Pier 1 Imports Recalls Bistro Chairs Due to Fall Hazard

    Pier 1 Imports is recalling Neely and Dahlia bistro chairs because loose bolts can cause the legs to collapse, posing a fall hazard.

    Product
    Neely and Dahlia Bistro Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V157000·2017-03-09

    Manac Recalls 2016-2017 Van Trailers Due to Failing Rub Rail Rivets

    Manac is recalling 2016-2017 Van Trailers because aluminum rivets securing external rub rails may fail, allowing the rails to detach and become road hazards.

    Product
    MANAC — MANAC VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0505-2017·2017-03-08

    Pacific Medical Solutions Recalls Nano PNC Water Due to Bacterial Contamination

    Pacific Medical Solutions is recalling Nano PNC Water because it was marketed without FDA approval and tested positive for the bacterium variovorax paradoxus.

    Product
    Nano PNC Water, packaged in amber glass bottles, Rx only, ICRPstudy.com, Immune Cellular Restoration Program.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0496-2017·2017-03-08

    United Exchange Recalls Non-Sterile Eye Wash Bottles Nationwide

    United Exchange Corporation is recalling 46,080 bottles of Eye Wash due to direct evidence of non-sterility contamination in two lots.

    Product
    EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1251-2017·2017-03-08

    Olympus Recalls URF-P6 Uretero-reno Fiberscopes Due to Tissue Trauma Risk

    Olympus is recalling URF-P6 and URF-P6R uretero-reno fiberscopes due to adverse events involving tissue trauma and stuck insertion tubes reported in similar devices.

    Product
    URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V152000·2017-03-08

    Hyundai Recalls Sonata Models Due to Front Seat Belt Defect

    Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles because front seat belt linkages may detach from anchor pretensioners, increasing injury risk in crashes.

    Product
    HYUNDAI — HYUNDAI SONATA HYBRID, SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0499-2017·2017-03-08

    United Exchange Recalls Eye Wash Bottles Due to Sterility Concerns

    United Exchange Corporation is recalling 190,710 bottles of Eye Wash due to a lack of assurance of sterility. The product was distributed nationwide, in Puerto Rico, and in Guyana.

    Product
    EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0788-2017·2017-03-08

    Medtronic SynchroMed II Software Card Recall for Priming Bolus Function

    Medtronic is recalling 22,298 SynchroMed II software application cards to update the priming bolus function and pump labeling.

    Product
    Medtronic SynchroMed II Implantable Drug Infusion System. This system includes: Model 8870 Software Application Card, Model 8840 N'Vision Clinician Programmer, and Model 8637 SynchroMed II Implantable Drug Infusion Pump (supplied in 20 ml or 40 ml reservoir size.) Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0497-2017·2017-03-08

    United Exchange Recalls Eye Irrigating Solution Due to Sterility Concerns

    United Exchange Corporation is recalling 112,320 bottles of Eye Irrigating Solution because the product lacks assurance of sterility.

    Product
    Eye Irrigating Solution, 4 fl oz (118 mL) bottle, OTC, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0536-1083-97
    Category
    Drug
    Distribution
    Distributed nationwide