The Recall Desk

State

US Virgin Islands product recalls

73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30351–30375 of 73896

  • HighNHTSA·20T002000·2020-02-04

    Goodyear Recalls Fortera HL Tires Due to Belt Separation Risk

    Goodyear is recalling specific Fortera HL tires because a manufacturing issue may cause belt separation, increasing the risk of a crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V060000·2020-01-31

    McElrath Trailers Recalls 2016-2020 Models Due to Frame Weld Cracks

    McElrath Trailers is recalling 2016-2020 VX30-800 and VX50-800 trailers because structural frame welds may crack, increasing crash risk.

    Product
    MCELRATH TRAILERS — MCELRATH TRAILERS VX50-800, VX30-800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V056000·2020-01-31

    Volkswagen Recalls Audi Vehicles for Driver Air Bag Inflator Defect

    Volkswagen Group of America is recalling specific Audi A8, A4, TT, and A6 models because driver air bag inflators may absorb moisture, potentially causing improper deployment in a crash.

    Product
    AUDI — AUDI A8, A4, TT, A6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V054000·2020-01-31

    Triple E Recalls 2020 Motorhomes Due to Propane Line Defects

    Triple E is recalling 237 2020 Unity, Wonder, and Serenity motorhomes because twisted or kinked propane lines may leak and cause a fire.

    Product
    WONDER — WONDER, UNITY, SERENITY W24RTB, W24MB, W24FTB, U24MB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V057000·2020-01-31

    Volkswagen Recalls 2018 Atlas Vehicles Due to Air Bag Sensor Defect

    Volkswagen is recalling 2018 Atlas vehicles because an incorrectly manufactured air bag sensor may delay or disable deployment, increasing injury risk in crashes.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V053000·2020-01-30

    Land Rover Recalls 2020 Discovery Models for Seat Frame Defect

    Jaguar Land Rover is recalling 2020 Discovery vehicles because second-row seat frames may lack fasteners, potentially failing to secure occupants in a crash.

    Product
    LAND ROVER — LAND ROVER DISCOVERY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V055000·2020-01-30

    GM Recalls 2019 Silverado and Sierra Trucks for Brake Software Error

    General Motors is recalling 2019 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because a software error may disable electronic brake assist, increasing crash risk.

    Product
    GMC — GMC, CHEVROLET SIERRA 1500, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20716·2020-01-30

    K-Apparel Recalls Children's Lounge Pants Due to Burn Hazard

    K-Apparel is recalling about 2,200 TINFL children's lounge pants because they fail federal flammability standards, posing a burn risk to children.

    Product
    Children's Lounge Pants
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20714·2020-01-30

    Polaris Recalls 2019 Pro XD Utility Vehicles Due to Rear Brake Failure Risk

    Polaris is recalling about 760 Model Year 2019 Pro XD utility vehicles because the rear brake line can puncture, causing rear brake failure and posing a crash hazard.

    Product
    Model Year 2019 Polaris PRO XD Utility Vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20713·2020-01-30

    Polaris Recalls 2017-2018 Brutus UTVs Due to Rear Brake Line Failure

    Polaris is recalling 2017-2018 Brutus utility vehicles because a rear brake line can puncture, causing brake failure and a crash hazard.

    Product
    Model Year 2017-2018 Brutus Utility Vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·005-2020·2020-01-29

    Banquet Pepperoni Stuffed Pizza Sandwiches Recalled for Undeclared Soy

    Astrochef LLC is recalling Banquet pepperoni stuffed pizza sandwiches due to misbranding and undeclared soy, a known allergen.

    Product
    Pegasus Foods Inc. — Astrochef LLC. Recalls Pepperoni Stuffed Pizza Sandwich Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0813-2020·2020-01-29

    GE Healthcare Recalls Carestation Anesthesia Systems Due to Loose Cable Connection

    GE Healthcare is recalling 3,319 Carestation anesthesia systems worldwide due to a potential loose cable connection that could cause loss of mechanical ventilation.

    Product
    Carestation 620/650/650c A1 Product Usage: anesthesia systems are intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (pediatric and adult.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0835-2020·2020-01-29

    Polymer Technology Systems Recalls CardioChek Plus Analyzers Due to Battery Overheating Risk

    Polymer Technology Systems is recalling 44,448 CardioChek Plus Professional Analyzers because a battery terminal defect can cause reverse contact and potential overheating.

    Product
    Henry Schein CardioChek Plus Professional Analyzer, New Analyzer, boxed, with carrying case, Reference Number 4060 HS, 570-0411
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0800-2020·2020-01-29

    Entropic Labs SARM RAD-140 Recalled for Lack of FDA Approval

    Entropic Labs is recalling SARM RAD-140 capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).

    Product
    Entropic Labs SARM RAD-140, 20mg Capsules, 30-count bottles, Entropic Labs UPC#: 651074545302
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0814-2020·2020-01-29

    GE Healthcare Recalls Carestation Anesthesia Systems Due to Loose Cable Risk

    GE Healthcare is recalling 280 Carestation anesthesia systems worldwide due to a potential loose cable connection that could cause a loss of mechanical ventilation.

    Product
    Carestation 620/650/650c A2 Product Usage: anesthesia systems are intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (pediatric and adult.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0794-2020·2020-01-29

    Denton Pharma Recalls Ranitidine Tablets Due to NDMA Impurity

    Denton Pharma is recalling 1,341 bottles of Ranitidine Tablets 150 mg because the product was found to contain the NDMA impurity.

    Product
    Ranitidine Tablets, USP 150 mg , a). 4 count bottle (NDC 70934-017-04), b). 20-count bottle (NDC 70934-017-20), c). 24-count bottle (NDC 70934-017-24) d). 30-count bottle (NDC 70934-017-30) e). 90-count bottle (NDC 70934-017-90), Rx Only, Repackaged by: Northwind Pharmaceuticals…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V049000·2020-01-29

    Forest River Recalls 2020 Recreational Trailers Due to Brake Switch Failure

    Forest River is recalling 218 units of 2020 recreational trailers because a failed break-away switch may prevent brakes from engaging if the trailer separates from the tow vehicle.

    Product
    FOREST RIVER — FOREST RIVER FREEDOM EXPRESS, WILDCAT MAXX, WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0795-2020·2020-01-29

    Denton Pharma Recalls Ranitidine Tablets Due to NDMA Impurity

    Denton Pharma is recalling 467 bottles of Ranitidine Tablets 300 mg because of the presence of NDMA impurity. The affected products were distributed nationwide.

    Product
    Ranitidine Tablets, USP 300 mg a). 15-count bottles (NDC 70934-287-15), b). 90-count bottles (NDC 70934-287-90), Rx Only, Repackaged by: Northwind Pharmaceuticals North Brenheim, NY 12131
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V050000·2020-01-29

    Vactor 2100i Vehicles Recalled for Safety Interlock Software Defect

    Vactor is recalling 2017-2020 2100i vehicles because a software defect may cause safety interlocks to fail, leading to unintentional vehicle movement and increased crash risk.

    Product
    VACTOR — VACTOR 2100I
    Category
    Vehicle
    Distribution
    Distributed nationwide