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.

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.

56226–56250 of 74005

  • SevereNHTSA·14V760000·2014-11-28

    Thomas Built Buses Recalls Minotour School Buses for Fuel Tank Strap Issue

    Daimler Trucks North America is recalling 2013-2015 Thomas Built Buses Minotour school buses because a loose fuel tank strap fastener could cause a fuel leak and fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V758000·2014-11-28

    Daimler Trucks Recalls 2015 Models Due to Brake Drag Risk

    Daimler Trucks North America is recalling 1,580 model year 2015 trucks because an improperly seated brake chamber diaphragm may cause brake drag, increasing the risk of a crash.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4700, COLUMBIA GLIDER, 108SD, CORONADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0252-2015·2014-11-26

    Abrams Royal Pharmacy Recalls Trace Mineral-5 MDV Due to Non-Sterility

    Abrams Royal Pharmacy is recalling Trace Mineral-5 MDV vials because a contract laboratory identified Staphylococcus warneri in the product, indicating non-sterility.

    Product
    Trace Mineral-5 MDV, supplied in 10 mL vials, Each ML contains: 1 mg Zinc (as sulfate), 0.4 mg Copper (as sulfate), 0.1 mg Manganese (as sulfate), 4 mcg Chromium (as chloride), 20 mcg Selenium (as sodium), 0.9% Benzyl alcohol in water for injection, Rx Only, Compounded…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0220-2015·2014-11-26

    Biomet Spine Recalls Durango Anchored ALIF Plate Due to Set Screw Risk

    Biomet Spine is voluntarily recalling 120 Durango Anchored ALIF Plate units because the set screw component may become dislodged from the plate assembly.

    Product
    LANX, REF, PCR8XXX-XXX, LOT, RXONLY. Packaged within aluminum sterilization case. Product Usage: The Durango implant is intended for spinal fusion procedures to be used with autogenous bone graft in skeletally mature patients with degenerative disc disease (DDD) at one or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0534-2015·2014-11-26

    InHarvest Garden Vegetable Seasoning Mix Recalled for Undeclared Milk

    InHarvest, Inc. is recalling Garden Vegetable Seasoning Mix because it contains milk, which is not declared on the label.

    Product
    Garden Vegetable seasoning Mix 12/4 oz. Product number 141000 Garden Vegetable seasoning mix. 4 oz..; Product number 14000 Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V756000·2014-11-26

    Fleetwood and Holiday Rambler RVs Recalled for Seat Mounting Defect

    Allied Recreation Group is recalling 2014-2015 Fleetwood Excursion and 2015 Holiday Rambler Ambassador vehicles because seat mounting brackets may be incorrectly installed, increasing crash injury risk.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER EXCURSION, AMBASSADOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0533-2015·2014-11-26

    InHarvest Garden Vegetable Seasoning Recalled for Undeclared Milk

    InHarvest is recalling Garden Vegetable Seasoning because it contains milk, which is not declared on the label.

    Product
    Whole Grain 5 Blend/Garden Vegetable 12/36 oz Product number 12410; Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed Corn Protein, Sun-Dried Tomato, Salt, Autolyzed Yeast…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0530-2015·2014-11-26

    InHarvest Garden Vegetable Seasoning Recalled for Undeclared Milk

    InHarvest, Inc. is recalling Garden Vegetable Seasoning mix because it contains milk, which is not declared on the label.

    Product
    White and Wild Medley/Garden Vegetable 12/36 oz; Product number 10410. Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed Corn Protein, Sun-Dried Tomato, Salt, Autolyzed Yeast…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0532-2015·2014-11-26

    InHarvest Garden Vegetable Seasoning Recalled for Undeclared Milk

    InHarvest, Inc. is recalling Rio Medley Garden Vegetable Seasoning because it contains milk, which is not declared on the label.

    Product
    Rio Medley/Garden Vegetable 12/36 oz; Product number 12310; Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed Corn Protein, Sun-Dried Tomato, Salt, Autolyzed Yeast Extract…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0531-2015·2014-11-26

    InHarvest Caviar Medley Garden Vegetable Seasoning Recalled for Undeclared Milk

    InHarvest, Inc. is recalling Caviar Medley Garden Vegetable products because the seasoning mix contains undeclared milk.

    Product
    Caviar Medley/Garden Vegetable 12/36 oz Product number 10610; Caviar Medley/Garden Vegetable 6/26 oz. Product number 10644 Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1578-2014·2014-11-26

    Medtronic Recalls Sterile Mouse Bags Due to Sterility Control Issues

    Medtronic Navigation is recalling sterile mouse bags because returned devices may not have been properly examined for damage that could compromise sterility.

    Product
    BAG 9732315 MOUSE STERILE 15 PK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14E080000·2014-11-26

    Cycle Gear Recalls Certain Street & Steel and Anarchy Motorcycle Helmets

    Cycle Gear is recalling specific Street & Steel Brotherhood and Anarchy motorcycle helmets that may not meet federal safety standards for impact protection.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1594-2014·2014-11-26

    Medtronic Recalls Non-Invasive Shunt Kits Due to Sterility Control Issues

    Medtronic Navigation is recalling 26,674 non-invasive shunt kits because returned devices were not adequately inspected for damage that could compromise sterility.

    Product
    SHUNT KIT 9733605 NON-INVASIVE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1600-2014·2014-11-26

    Medtronic Recalls Tumor Resection Kits Due to Sterility Control Issues

    Medtronic Navigation is recalling 26,674 Tumor Resection Kits because returned devices may not have been properly examined for damage to ensure sterility.

    Product
    TUMOR RESECTION KIT 9733607 NON-INVASIVE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1590-2014·2014-11-26

    Medtronic Recalls Spine Pedicle Accessory Kits Due to Sterility Concerns

    Medtronic Navigation is recalling 26,674 single-use spine pedicle accessory kits because returned devices may not have been properly examined for damage to ensure sterility.

    Product
    PAK 9733497 NAV NIM-SPINE PEDICLE ACC KT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1586-2014·2014-11-26

    Medtronic Recalls Instrument Trackers Due to Sterility Control Issues

    Medtronic Navigation is recalling single-use instrument trackers because returned devices may not have been properly examined for damage to ensure sterility.

    Product
    INSTRUMENT TRACKER 9733533XOM ENT 1PK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1602-2014·2014-11-26

    Medtronic Recalls Single-Use Navigation Devices Due to Sterility Control Issues

    Medtronic Navigation is recalling 26,674 single-use, disposable navigation devices because returned units were not adequately examined for damage that could compromise sterility.

    Product
    UPGRD PRGM 9734638 ADD AxiEM NAVIGATION
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1579-2014·2014-11-26

    Medtronic Recalls Biopsy Needle Kits Due to Sterility Control Issues

    Medtronic Navigation is recalling 26,674 biopsy needle kits because returned devices may not have been properly examined for damage to ensure sterility.

    Product
    BIOPSY NEEDLE KIT, 9733068, PASSIVE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0504-2015·2014-11-26

    Original Soup Man Recalls Lobster Bisque for Undeclared Seafood Allergens

    Original Soup Man is recalling Lobster Bisque due to undeclared shrimp, tilapia, and perch. Consumers should check lot numbers and stop consuming the product.

    Product
    THE ORIGINAL SOUPMAN Lobster Bisque, Net Wt 17 oz (482 g). Product is packed as a tetra pak and ships as a pack of 12 or 6 containers per carton. Distributed exclusively by: SoupMan Inc. Staten Island, NY 10314
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0221-2015·2014-11-26

    Elekta MOSAIQ Oncology System Recalled for Dose Rounding Error

    Elekta, Inc. is recalling 15 units of the MOSAIQ oncology information system because a dose rounding error may cause incorrect numeric data to be displayed on printed reports.

    Product
    MOSAIQ Product Usage: MOSAIQ is an oncology information system used to manage workflows for treatment planing and delivery. It supports information flow among healthcare facility personnel and can be used wherever radiotherapy and/or chemotherapy are prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0215-2015·2014-11-26

    Soma Access Systems Recalls AxoTrack I Sterile Procedure Kits

    Soma Access Systems is recalling 3,530 units of AxoTrack I Sterile Procedure Kits because the sterile packaging may fail before the expiration date.

    Product
    AxoTrack I Sterile Procedure Kit 18G, K1001-18XTW, (24/case labeled for US, 5/case labeled for US, 24/case labeled for EU, 5/case labeled for EU). Sterile Procedure Kit for use AxoTrack enabled Ultrasound Transducer for magnetic needle tracking.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1585-2014·2014-11-26

    Medtronic Recalls Single-Use Ref Frame Driver Kits Due to Sterility Concerns

    Medtronic Navigation is recalling 26,674 single-use Ref Frame Driver Kits because returned devices may not have been properly examined for damage to ensure sterility.

    Product
    INST 9731132 KIT CR REF FRAME DRIVER 5PK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0235-2015·2014-11-26

    Siemens SimView NT Simulation System Recalled for Movement Control Defect

    Siemens is recalling six SimView NT simulation systems because a rare defect may prevent components from stopping, risking collision with patients or equipment.

    Product
    Siemens SimView NT and SimView NT with IDI simulation system components: Product Usage: The intended use of the Radiation Therapy Simulation system is used for simulation of treatment planning prior to the therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide