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.

56801–56825 of 74005

  • ModerateFDA (Food)·F-0011-2015·2014-10-15

    Hostess Frosted Bagged Donettes Recalled for Potential Mold Growth

    Hostess Brands LLC is recalling specific frozen donettes due to potential mold growth caused by higher-than-average moisture content.

    Product
    Hostess Frosted Bagged Donettes- FROZEN ONLY, 11.25 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0033-2015·2014-10-15

    Navilyst Medical Recalls PICC Kits Due to Potential Sterility Compromise

    Navilyst Medical is recalling specific PICC Convenience Kits because they contain BD syringes with open seals that may affect sterility.

    Product
    PICC Convenience Kit with Accessories, BioFlo PICC with ENDEXO and PASV Valve Technology, 4F-55 cm SINGLE LUMEN, UPN Product No. H96560M0501981, REF/Catalog No. 60M050198, STERILE --- Intended for short or long-term peripheral access to the central venous system for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0009-2015·2014-10-15

    Hostess Powdered Bagged Donettes Recalled for Potential Mold Growth

    Hostess Brands LLC is recalling 17,330 units of Powdered Bagged Donettes due to potential mold growth caused by higher-than-average moisture content.

    Product
    Hostess Powdered Bagged Donettes, 10.5 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0024-2015·2014-10-15

    Siemens Recalls Dimension Vista Mass CKMB Isoenzyme Calibrator Due to Drift

    Siemens Healthcare Diagnostics is recalling Dimension Vista Mass CKMB Isoenzyme Calibrators because routine stability monitoring showed drift exceeding acceptance criteria.

    Product
    Dimension Vista¿ Mass CKMB Isoenzyme Calibrator (MMB CAL) an in vitro diagnostic product for the calibration of Creatine Kinase MB Isoenzyme (MMB) method on the Dimension Vista¿ System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0041-2015·2014-10-15

    Smith & Nephew Recalls RENASYS EZ Canisters Due to Deformed Inlet Ports

    Smith & Nephew is recalling RENASYS EZ and EZ Plus 800 mL canisters with deformed inlet ports on the lid. The defect may affect the collection of wound exudate during negative pressure wound therapy.

    Product
    RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) with Solidifier Product Usage: RENASYS EZ and RENASYS EZ Plus Canisters are used for the collection of exudate removed from wounds being treated by negative pressure wound therapy (NPWT).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0008-2015·2014-10-15

    Hostess Frosted Bagged Donettes Recalled for Potential Mold Growth

    Hostess Brands LLC is recalling Frosted Bagged Donettes due to potential mold growth caused by higher-than-average moisture content.

    Product
    Hostess Frosted Bagged Donettes, 11.25 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0030-2015·2014-10-15

    Navilyst Medical Recalls PICC Kits Due to Potential Sterility Compromise

    Navilyst Medical is recalling specific PICC Convenience Kits because they contain BD syringes with open seals that may affect sterility.

    Product
    PICC Convenience Kit with Accessories, BioFlo PICC with ENDEXO and PASV Valve Technology, 4F-55 cm SINGLE LUMEN, UPN Product No. H96560M1841541, REF/Catalog No. 60M184154, STERILE --- Navilyst Medical, Inc. 10 Glens Falls Technical Park Glens Falls, NY 12801
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0010-2015·2014-10-15

    Hostess Powdered Donettes Recalled for Potential Mold Growth

    Hostess Brands LLC is recalling specific lots of Powdered Single-Serve Donettes due to higher-than-average moisture content that may allow mold growth.

    Product
    Hostess Powdered Single-Serve Donettes, 3 oz., 6 ct.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0012-2015·2014-10-15

    Hostess Recalls Frozen Donettes Due to Potential Mold Growth

    Hostess Brands LLC is recalling specific lots of frozen Donettes because laboratory analysis found higher-than-average moisture content, creating a potential for mold growth.

    Product
    Hostess Powdered Bagged Donettes- FROZEN ONLY, 10.5 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0010-2015·2014-10-15

    VistaPharm Recalls Metoclopramide Oral Solution Due to Leaking Containers

    VistaPharm is recalling 322,650 cups of Metoclopramide Oral Solution because the containers leak when inverted.

    Product
    METOCLOPRAMIDE ORAL SOLUTION, USP 5 mg/5 mL, (present as the hydrochloride), 10 mL cups, Rx only. Manufactured by VistaPharm Inc., Largo, FL 33771. NDC 66689-031-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0008-2015·2014-10-15

    Astellas Recalls Tarceva Tablets Due to Failed Dissolution Specifications

    Astellas Pharma US Inc is recalling 9,236 bottles of Tarceva (erlotinib) 150 mg tablets because they failed routine stability testing for dissolution.

    Product
    Tarceva (erlotinib) Tablets, 150 mg, 30 count bottle, Rx only, Manufactured by: Kremers Urban Pharmaceuticals Inc. Seymour, IN 47274 NDC 50242-064-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0035-2015·2014-10-15

    Navilyst Medical Recalls PICC Kits Due to Potential Sterility Issues

    Navilyst Medical is recalling specific PICC Convenience Kits because they contain BD syringes with open seals that may compromise sterility.

    Product
    PICC Convenience Kit with Accessories, BioFlo PICC with ENDEXO Technology, 5F-55 cm DUAL LUMEN, UPN Product No. H96560M0367051, REF/Catalog No. 60M036705, STERILE --- Intended for short or long term peripheral access to the central venous system for intravenous therapy…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0013-2015·2014-10-15

    Gilead Recalls Truvada Tablets Due to Silicone Rubber Particulates

    Gilead Sciences is recalling Truvada tablets because they contain small red silicone rubber particulates. The recall affects 10,317 bottles distributed nationwide.

    Product
    TRUVADA — TRUVADA (EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0014-2015·2014-10-15

    Bracco Recalls E-Z-GAS Antacid Due to Subpotent Drug Levels

    Bracco Diagnostic Inc is recalling E-Z-GAS antacid packets because routine stability testing found the drug to be subpotent.

    Product
    E-Z-GAS — E-Z-GAS (ANTACID/ANTIFLATULENT)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V643000·2014-10-14

    Chrysler Recalls 2014 Dodge Durango and Jeep Grand Cherokee for Airbag Fault

    Chrysler is recalling 2014 Dodge Durango and Jeep Grand Cherokee vehicles because a module fault may disable airbags and seat belt pretensioners, increasing injury risk in crashes.

    Product
    DODGE — DODGE, JEEP DURANGO, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V646000·2014-10-14

    Vermeer Recalls 2014 TR620 Trailers Due to Hitch Mount Defect

    Vermeer is recalling 2014 TR620 Trommel trailers because an incorrect material in the pintle hitch mount may allow bolts to loosen, increasing crash risk.

    Product
    VERMEER — VERMEER TR620
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V638000·2014-10-10

    Strick Dry Freight Van Trailers Recalled for Rear Impact Guard Defect

    Strick Trailers is recalling 2009-2015 Dry Freight Van Trailers because rear impact guards do not meet federal safety standards, increasing injury risk in crashes.

    Product
    STRICK — STRICK DRY FREIGHT VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V642000·2014-10-10

    Wheeled Coach Recalls Ambulances Due to Suspension Tank Mount Failure Risk

    Wheeled Coach is recalling certain 2013-2015 ambulances because a suspension fluid tank mount may fail, causing the tank to separate and create a road hazard.

    Product
    WHEELED COACH — WHEELED COACH TYPE III AMBULANCE, TYPE I AMBULANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V639000·2014-10-10

    Acura Recalls MDX and RLX Models for Seat Belt Malfunction

    Honda is recalling 2014-2015 Acura MDX and 2014 RLX vehicles because seat belts may not extend or retract in low temperatures, increasing crash injury risk.

    Product
    ACURA — ACURA MDX, RLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E068000·2014-10-10

    Eaton Fuller 365mm Clutch Recall for Disengagement Failure

    Eaton is recalling 574 Fuller 365mm clutches manufactured in 2014 due to a defective bearing that may prevent disengagement, increasing crash risk.

    Product
    POWER TRAIN:CLUTCH ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V640000·2014-10-10

    Keystone Recalls 2015 Dutchmen Rubicon Trailers Due to Fuel Line Defect

    Keystone RV Company is recalling 2015 Dutchmen Rubicon trailers because an incorrectly installed fuel line clamp may cause the line to disconnect, potentially leading to a fuel leak and fire.

    Product
    DUTCHMEN — DUTCHMEN RUBICON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V637000·2014-10-10

    Goshen Buses Recalled for Wheelchair Lift Platform Cracking Risk

    Goshen Coach is recalling certain buses because wheelchair lift platform side plates may crack, posing an injury risk to operators.

    Product
    GOSHEN — GOSHEN GCII, SENTINEL, SENTRY, PACER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V641000·2014-10-10

    Mobility Works Recalls Ford Vans with Cracking Wheelchair Lifts

    Mobility Works is recalling 834 Ford E-Series vans modified with Ricon wheelchair lifts. The platform side plates may crack, causing the lift to fall and injure the operator.

    Product
    FORD — FORD, MOBILITY WORKS E150, E250, E350, fORD E-150
    Category
    Vehicle
    Distribution
    Distributed nationwide