The Recall Desk

State

US Virgin Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50601–50625 of 73995

  • LowFDA (Devices)·Z-0457-2016·2015-12-30

    BC Group International Recalls Defibrillator and Pacer Analyzer Units

    BC Group International is recalling five DA-2006P Defibrillator / Pacer Analyzer units because reversed wires cause inverted waveforms.

    Product
    DA-2006P - Defibrillator / Pacer Analyzer; Product Usage: Intended to measure the output of a defibrillator or transcutaneous pacemaker.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V883000·2015-12-29

    Micro Bird Recalls 2014-2016 School Buses for Loose Wheel Bolts

    Micro Bird is recalling 464 school buses because a camber caster kit bolt may be insufficiently torqued, posing a risk of vehicle misalignment and loss of control.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS, G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V884000·2015-12-29

    Micro Bird Recalls Transit Buses Due to Loose Wheel Bolt

    Micro Bird is recalling 2014-2016 G5 and MB II transit buses because a wheel bolt may be insufficiently torqued, posing a risk of vehicle misalignment and loss of control.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V881000·2015-12-28

    Ferrari Recalls 2016 488 GTB Vehicles for Fuel Line Fire Risk

    Ferrari is recalling 119 model year 2016 488 GTB vehicles because a fuel line connection may leak vapor, increasing fire risk.

    Product
    FERRARI — FERRARI 488 GTB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V880000·2015-12-28

    Tiffin Motorhomes Recall 2007-2015 Models Due to Unstable Entry Steps

    Tiffin is recalling 2007-2015 motorhomes because a bolt on the electric steps may fracture, causing the steps to become unstable and increasing the risk of injury.

    Product
    TIFFIN — TIFFIN ALLEGRO, ALLEGRO BAY, BAY, PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0417-2016·2015-12-23

    Ashdon Farms Honey Mustard Mix Recalled for Missing Milk Allergen Labeling

    A. L. Schutzman Company, Inc. is recalling Ashdon Farms Honey Mustard Mix because the packaging lists whey but fails to declare milk in the 'Contains' statement.

    Product
    Honey Mustard Mix sold under the following brand: Ashdon Farms, Net Wt. 8 oz. (227 g), UPC 79113-41184
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0415-2016·2015-12-23

    Zenobia Recalls Flax Seed Meal Due to Possible Salmonella Presence

    Zenobia Co. is recalling My Spice Sage Ground Flax Seed Meal due to the possible presence of Salmonella. The product was sold nationwide via the internet.

    Product
    My Spice Sage Ground Flax Seed Meal under the following labels: 1) NET WT 4 oz. (113g) UPC# 00575004, 2) NET WT 16 oz. (454g) UPC# 00575016, 3) NET WT 50 pounds UPC# 00575111.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0443-2016·2015-12-23

    Remel Recalls Gentamicin Antimicrobial Susceptibility Testing Discs

    Remel Inc is recalling specific lots of Gentamicin Antimicrobial Susceptibility Testing Discs because the antibiotic concentration may be insufficient, potentially leading to incorrect test results.

    Product
    Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10), REF# CT0024B packaged in packs of 5 cartridges - 50 disc/cartridge. Used in the semi-quantitative agar diffusion test method for in vitro susceptibility testing to assist in the determination of a suitable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V878000·2015-12-23

    2015 Jeep Compass and Patriot Recalled for Power Steering Hose Defect

    Chrysler is recalling 2015 Jeep Compass and Patriot vehicles because a power steering hose clamp may be installed incorrectly, increasing the risk of a fire.

    Product
    JEEP — JEEP PATRIOT, COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0394-2016·2015-12-23

    Insulet Recalls OmniPod Insulin Management System Due to Needle Deployment Failure

    Insulet Corporation is recalling 5,179 boxes of OmniPod Insulin Management Systems because the needle mechanism may fail to deploy or deploy with a delay.

    Product
    OmniPod¿, Insulin Management System (OUS) Catalog Number: 14810 Product Usage: The OmnniPod¿ Insulin Management System is intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin and for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0416-2016·2015-12-23

    Girl Scouts Honey Mustard Pretzel Mix Recalled for Milk Allergen Mislabeling

    A. L. Schutzman Company, Inc. is recalling Girl Scouts Honey Mustard Pretzel Mix because the product lists whey but fails to declare milk in the 'Contains' statement.

    Product
    Honey Mustard Pretzel Mix sold under the following brand and size: Girl Scouts, NET WT 7 oz. (198g).
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0393-2016·2015-12-23

    Insulet Recalls OmniPod Insulin Systems Due to Needle Deployment Failure

    Insulet Corporation is recalling OmniPod Insulin Management Systems because the needle mechanism may fail to deploy or deploy with a delay.

    Product
    OmniPod¿, Insulin Management System (US) Catalog Number: PODZXP420 Product Usage: The OmnniPod¿ Insulin Management System is intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin and for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0414-2016·2015-12-23

    GE Healthcare Optima IGS 320 Recall for Loss of Displayed Imaging

    GE Medical Systems is recalling 45 Optima IGS 320 systems due to a potential safety issue involving non-recoverable loss of displayed imaging.

    Product
    GE Healthcare Optima IGS 320. Product Usage: The angiographic X-ray systems are indicated for use for patients from newborn to geriatric in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular and non-vascular, diagnostic and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V870000·2015-12-23

    Navistar Recalls IC Bus Transit Models Due to Wheelchair Lift Defect

    Navistar is recalling certain 2007-2015 IC Bus transit models because wheelchair lift bearings may move out of position, causing the platform to fall.

    Product
    IC BUS — IC BUS CE, FECB, FE, RE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V873000·2015-12-23

    H&H Trailers Recall 2015-2016 Utility and Bike Trailers for Hinge Defect

    H&H Trailers is recalling 1,847 model year 2015-2016 trailers because aluminum gate hinges may bend or break, potentially causing the gate to open unexpectedly.

    Product
    H&H — H&H RSA RAIL SIDE TANDEM AXLE, SSA SOLID SIDE TANDEM, AMS BIKE TRAILER, SSA SOLID SIDE SINGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0417-2016·2015-12-23

    Stryker Guidewire Introducer Needles Recalled for Expiration Date Issues

    Stryker is recalling 120 units of Guidewire Introducer Needles shipped after expiration or with minimal time remaining due to infection risk.

    Product
    Cournand Modified 2-PC 19G, 5.4cm or (Guidewire Introducer Needle) 20 units per case The Stryker Guidewire Introducer Needles are designed for the percutaneous puncture of the anterior/posterior wall of a blood vessel. This provides an entry for a guidewire, vessel dilator…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0420-2016·2015-12-23

    Verathon GlideScope Video Laryngoscope Blades Recalled for Potential Separation

    Verathon is recalling GlideScope Video Laryngoscope blades because silicone adhesive may fail, causing the blade halves to separate during use.

    Product
    GlideScope Video Laryngoscope (GVL), Part Number GVL 3 - 0574-0007; GVL 4 - 0574-0001; GVL 5- 0574-0030. The system consists of a video laryngoscope and portable video monitor. The GlideScope Video Laryngoscopes are intended for use by qualified medical professionals to obtain…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0425-2016·2015-12-23

    bioMerieux MYLA Clinic Patch 3.2.0 CD Recall for Patient Data Linking Error

    bioMerieux, Inc. is recalling MYLA Clinic Patch 3.2.0 CD software because it may link test results to incorrect patient records when connected to specific laboratory systems.

    Product
    MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology which: Interfaces between the instruments connected to the application and the LIS(s) (Laboratory Information System(s)).
    Category
    Medical Device
    Distribution
    Distributed nationwide