The Recall Desk

State

US Virgin Islands product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26101–26125 of 73744

  • HighNHTSA·21V061000·2021-02-08

    2021 PJ Trailers C5, C4, U8, and other models recalled for missing axle bearings

    Certain 2021 PJ Trailers models (C5, C4, U8, UL, U6, UC) are recalled because their suspension axles may have missing inner bearings that could cause wheel separation and increase crash risk.

    Product
    PJ TRAILERS — PJ TRAILERS U6, C4, UL, C5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·21V050000·2021-02-05

    GM Recalls Trucks and SUVs for Airbag Inflator Explosion Risk

    General Motors is recalling specific 2007-2011 trucks and SUVs because the front passenger airbag inflators may explode due to humidity, posing a risk of serious injury or death.

    Product
    GMC — GMC, CHEVROLET, CADILLAC SIERRA 2500, AVALANCHE, ESCALADE EXT, ESCALADE ESV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·21V051000·2021-02-05

    GM Recalls 2012 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling 2012 Chevrolet, GMC, and Cadillac vehicles because the front passenger airbag inflators may explode, posing a risk of serious injury or death.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SILVERADO 1500, SILVERADO 3500, YUKON, ESCALADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·21V053000·2021-02-05

    GM Recalls 2009-2013 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling specific 2009-2013 Chevrolet, GMC, and Cadillac vehicles because the front passenger airbag inflator may explode, sending metal fragments into the cabin.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC TAHOE, YUKON XL, SIERRA 1500, ESCALADE ESV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V057000·2021-02-05

    Mercedes-Benz Recalls GLE and GLS Models for Dashboard Defect

    Mercedes-Benz is recalling 2020-2021 GLE and GLS models because the dashboard may not be properly secured, which could impair airbag inflation in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450, GLS 450, AMG GLE53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V052000·2021-02-05

    GM Recalls 2007-2009 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling specific 2007-2009 Chevrolet, Cadillac, and GMC vehicles because the front passenger airbag inflators may explode, posing a risk of serious injury or death.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, GMC SUBURBAN, ESCALADE ESV, ESCALADE EXT, AVALANCHE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V054000·2021-02-05

    GM Recalls 2010-2014 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling specific 2010-2014 Cadillac, Chevrolet, and GMC vehicles because the front passenger airbag inflators may explode due to propellant degradation.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE EXT, SUBURBAN, TAHOE, SIERRA 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V055000·2021-02-05

    Mercedes-Benz Metris and Sprinter Recall for eCall Software Defect

    Daimler Vans USA is recalling 2016-2020 Metris and 2019-2020 Sprinter vans because the eCall system may send emergency responders to the wrong location after a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS, SPRINTER 1500, SPRINTER 2500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V058000·2021-02-05

    Mercedes-Benz vehicles recall: eCall software may fail to report correct crash location

    Mercedes-Benz is recalling 2016-2021 vehicles with eCall software that may fail to communicate the correct crash location to emergency services, potentially delaying emergency response.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH AMG CLA45, CLS 450, AMG S63, AMG GT43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V056000·2021-02-05

    Mercedes-Benz Recalls 2020 GLE Models for Reverse Light Malfunction

    Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because a lighting control unit malfunction may leave the left reverse light on in other gears, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V049000·2021-02-04

    Jayco Eagle Fifth Wheel Recall for Incorrect Spring Hanger

    Jayco is recalling 2021 Eagle fifth wheel vehicles equipped with incorrect spring hangers that reduce tire clearance, increasing the risk of tire blowouts.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V046000·2021-02-03

    BMW Recalls 2020-2021 Models for Driveshaft Breakage Risk

    BMW is recalling specific 2020-2021 530i, 540i, and 740Li vehicles because output shafts may break due to a manufacturing error, potentially causing loss of drive power or rollaway.

    Product
    BMW — BMW 530I, 540I, 740LI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0240-2021·2021-02-03

    IMC Wash-Free Hand Sanitizer Recalled for Methanol Contamination

    Shane Erickson Inc is recalling IMC Wash-Free Hand Sanitizer because it was manufactured at a facility that produced subpotent products containing methanol.

    Product
    IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 3.4 fl. oz. (100 ml), Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384. Labeled as a) SAFE-GUARD Products International, b) Safe-WAY JEVCO Wash-Free Hand Sanitizer, c) TRACTION CAPITAL, d) United…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0239-2021·2021-02-03

    IMC Wash-Free Hand Sanitizer Recalled for Methanol Contamination

    Shane Erickson Inc is recalling IMC Wash-Free Hand Sanitizer because it was manufactured at a facility that produced subpotent product containing methanol.

    Product
    IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 1.7 fl. oz. (50 ml) bottles, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384, Made in China, ALSO distributed with Custom front labels as follows a) Sadie G. Mays Health & Rehabilitation Center, b) Pacers logo, c)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0241-2021·2021-02-03

    IMC Wash-Free Hand Sanitizer Recalled for Methanol Contamination

    Shane Erickson Inc is recalling IMC Wash-Free Hand Sanitizer because it was produced at a facility that manufactured subpotent products containing methanol.

    Product
    IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 10.1 fl. oz. (300 ml), Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384. Labeled as Thrifty White Pharmacy Wash-Free Hand Sanitizer. UPC 8 19845 00599 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0903-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Navigation Ring Defects

    Respironics is recalling 9,856 V60 Ventilators worldwide due to navigation ring issues that may cause erratic parameter changes or inoperability.

    Product
    Philips Respironics V60 Ventilator Part Number 1053614 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0916-2021·2021-02-03

    Philips Respironics V60 Ventilator Recall for Navigation Ring Defects

    Respironics is recalling V60 ventilators because the navigation ring may fail or cause erratic parameter changes.

    Product
    Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories. Philips Respironics V60 Ventilator Part Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0904-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Navigation Ring and Liquid Ingress Issues

    Respironics is recalling 934 V60 Ventilators worldwide due to potential navigation ring malfunctions and liquid ingress risks.

    Product
    Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0885-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk

    Respironics is recalling 2,144 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.

    Product
    Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0911-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Navigation Ring Defect

    Respironics is recalling 10,291 V60 ventilators worldwide due to a navigation ring that may fail or cause erratic parameter changes.

    Product
    Philips Respironics V60 Ventilator Part Number 1076716 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide