The Recall Desk

State

US Virgin Islands product recalls

73,809 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45801–45825 of 73987

  • LowFDA (Drugs)·D-0122-2017·2016-11-09

    Par Pharmaceutical Recalls Subpotent Gildess FE 1.5/30 Oral Contraceptive Tablets

    Par Pharmaceutical is recalling Gildess FE 1.5/30 tablets because they may contain subpotent levels of ethinyl estradiol.

    Product
    Gildess FE 1.5/30 (norethindrone acetate, 1.5 mg and ethinyl estradiol tablets, 0.03 mg, USP and ferrous fumarate tablets, USP 75 mg), 6 blisters (28 count), NDC 0603-7608-17, Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·105-2016·2016-11-08

    Water Lilies Food Recalls Egg Rolls Due to Undeclared Shrimp Allergen

    Water Lilies Food Inc. is recalling approximately 1,710 pounds of egg rolls because they contain undeclared shrimp and are mislabeled as pork.

    Product
    Water Lilies Food, LLC — Water Lilies Food Inc. Recalls Egg Roll Product Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V810000·2016-11-08

    Newmar Recalls 2017 Motorhomes Due to Throttle Circuit Wire Interference

    Newmar is recalling 51 model year 2017 motorhomes because throttle circuit wires may not be twisted, potentially causing unintended acceleration or deceleration.

    Product
    NEWMAR — NEWMAR LONDON AIRE, MOUNTAIN AIRE, KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V812000·2016-11-08

    Hyundai Translead Recalls 2012-2013 HT Trailers Due to Cracking I-Beams

    Hyundai Translead is recalling 892 model year 2012-2013 HT trailers because I-beams may crack, potentially causing the bogie to detach and increasing crash risk.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD HT HYCUBE, HT ORIGINAL, HT COMPOSITE-XT, HT COMPOSITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17709·2016-11-08

    Trane Recalls Furnaces Due to Electrical Shock Hazard

    Trane is recalling about 17,700 furnaces because a loose ground wire creates a shock hazard if an electrical component fails.

    Product
    Furnaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V813000·2016-11-08

    Chrysler Recalls 2016 Dodge Dart for Windshield Wiper Circuit Failure

    Chrysler is recalling 53,155 2016 Dodge Dart vehicles because a faulty washer pump can cause the wiper circuit to fail, reducing visibility and increasing crash risk.

    Product
    DODGE — DODGE DART
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V809000·2016-11-07

    Daimler Trucks Recalls 2016-2017 FCCC Chassis for Fire Risk

    Daimler Trucks is recalling 1,827 model year 2016-2017 FCCC recreational vehicle chassis because an incorrectly routed power steering hose may cause electrical arcing and a fire.

    Product
    FCCC — FCCC XCR, XCM, XCL, XBR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V806000·2016-11-07

    Terex Advance Front Discharge Concrete Mixers Recalled for Axle Defect

    Terex Advance is recalling 2016-2017 Front Discharge Concrete Mixers because a front axle king-pin may fracture, potentially causing wheel separation and loss of vehicle control.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE CONCRETE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V802000·2016-11-04

    GM Recalls 2017 Cadillac XT5 and GMC Acadia for Brake Caliper Defect

    General Motors is recalling 2017 Cadillac XT5 and GMC Acadia vehicles because front brake caliper seals may leak fluid, reducing braking performance.

    Product
    CADILLAC — CADILLAC, GMC XT5, ACADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V804000·2016-11-04

    PTIC Recalls Stratos Asphalt Distributor Trailers Due to Axle Overload Risk

    PTIC is recalling 2014-2016 Stratos asphalt distributor trailers because fully loaded weight may exceed axle capacity, risking bearing overheating or hub detachment.

    Product
    STRATOS — STRATOS DMD-1000, DMT-1000, DMD-600, DMD-400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V803000·2016-11-04

    PACCAR Recalls 2017 Peterbilt and Kenworth Trucks for Tire Defect

    PACCAR is recalling 2017 Peterbilt and Kenworth trucks equipped with specific Goodyear tires that may partially separate, increasing crash risk.

    Product
    PETERBILT — PETERBILT, KENWORTH 389, 337, 330, T660
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V805000·2016-11-04

    Terex Recalls 2009-2014 TC and TCX Trucks for Wiring Defect

    Terex is recalling 2009-2014 TC and TCX hybrid electric trucks because improper wiring may cause the aerial boom to move unintentionally, increasing the risk of injury.

    Product
    TEREX — TEREX TC, TCX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V801000·2016-11-03

    E-One Recalls 2014-2016 Fire Trucks Due to Hydraulic Leak Risk

    E-One is recalling 2014-2016 Typhoon, Quest, and Cyclone fire trucks equipped with aerial ladders because a filter design change may cause hydraulic fluid leaks.

    Product
    E-ONE — E-ONE QUEST, TYPHOON, CYCLONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17027·2016-11-03

    KTM and Husqvarna Recall Off-Road Motorcycles Due to Brake Malfunction

    KTM North America is recalling about 1,200 model year 2017 KTM and Husqvarna off-road motorcycles because the front brake master cylinder can malfunction, posing a crash hazard.

    Product
    Closed-course/competition off-road motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0116-2017·2016-11-02

    St Jude Medical Recalls Implantable Defibrillators Due to Battery Defect

    St Jude Medical is recalling specific implantable defibrillators because a lithium cluster in the battery can cause a short circuit and premature depletion.

    Product
    Unify, Model No. CD3231-40, CD3231-40Q. Unify Quadra, Model No. CD3249-40, CD3249-40Q. Unify Assura, Model No. CD3257-40, CD3357-40C, CD3357-40Q. Fortify and Fortify Assura implantable cardioverter defibrillators (ICDS) are intended to provided ventricular anti-tachycardia…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0097-2017·2016-11-02

    Roche Recalls cobas 8000 Analyzers Due to Sharp Edge Injury Reports

    Roche is recalling cobas 8000 Modular Analyzers and e602 Immunoassay Analyzers after four reports of injury caused by a sharp edge on the sample rack tray.

    Product
    cobas 8000 Modular Analyzer Series c8000, Chemistry (Photometric, Discrete) for clinical use Modular e602: Immunoassay Analyzer Product Usage: The VS II system is a stand-alone, computer-controlled instrument designed to aliquot patient sample from a primary tube to a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0300-2017·2016-11-02

    Ortho-Clinical Diagnostics Recalls enGen Laboratory Automation System Due to Sample Error

    Ortho-Clinical Diagnostics is recalling the enGen Laboratory Automation System because a software error may cause sample identification to be mismatched with assay results.

    Product
    enGen Laboratory Automation System (Product Code ENGEN) configured with Thermo Scientific Centrifuge Module and TCAutomation Software Version 3.6.1 and Below; IVD. --- Thermo Scientific Centrifuge Module has Product Code 952040-EG 6844097. The VITROS 5,1 FS Chemistry System…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0109-2017·2016-11-02

    Roche Recalls cobas p 312 Pre-Analytical System Calculator Modules

    Roche is recalling 9,014 cobas p 312 Pre-Analytical System calculator/data processing modules due to four reported injuries caused by a sharp edge on the sample rack tray.

    Product
    cobas p 312 Pre-Analytical System calculator/data processing module, for clinical use Product Usage: The cobas p471 system is an automatic centrifuge module for centrifuging primary sample tubes, which will then be transported to the output module.
    Category
    Medical Device
    Distribution
    Distributed nationwide