The Recall Desk

State

US Virgin Islands product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27701–27725 of 73754

  • CriticalFDA (Drugs)·D-1574-2020·2020-09-09

    FDA Recalls Skin Guard 24 Hand Sanitizing Towelettes for Unapproved Methanol

    SG24 LLC is recalling Skin Guard 24 hand sanitizing towelettes because they contain unapproved methanol and lack FDA approval.

    Product
    Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Towelette packaged in 2.5 x 3.75 packets, Dist by: SG24 LLC, Bolingbroke, GA 31004
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1355-2020·2020-09-09

    Whole Foods Market Artequeso Manchego Cheese Recalled for Undeclared Egg

    Whole Foods Market is recalling Artequeso Manchego cheese due to undeclared lysozyme from egg whites, a common allergen.

    Product
    Whole Foods Market Artequeso Manchego 6 month aged raw Raw Milk - Aged 60 days or more PLU 20057900000 Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1362-2020·2020-09-09

    Whole Foods Market Recalls Piave Vecchio Cheese for Undeclared Egg

    Whole Foods Market is recalling Piave Vecchio cheese nationwide due to undeclared egg whites (lysozyme). Consumers with egg allergies should not consume the product.

    Product
    Whole Foods Market AGRIFORM PIAVE VECCHIO PLU 29336200000 Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1357-2020·2020-09-09

    Whole Foods Market Recalls Raw Milk Cheese Due to Undeclared Egg Allergen

    Whole Foods Market is recalling Mitica La Dama Sagrada Raw Milk cheese because it contains undeclared lysozyme from egg whites.

    Product
    Whole Foods Market Mitica La Dama Sagrada Raw Milk - Aged 60 Days or More PLU 20656400000 Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1360-2020·2020-09-09

    Whole Foods Market Recalls Sliced Cheese for Undeclared Egg Allergen

    Whole Foods Market is recalling specific sliced cheese products because they contain undeclared lysozyme from egg whites, posing a risk to individuals with egg allergies.

    Product
    Whole Foods Market Chimay Grand Cru PLU 29388800000 and Whole Foods Market Lactalis MIMOLETTE Aged 12 MONTHS PLU 25704400000 Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1571-2020·2020-09-09

    SkinGuard 24 Hand Sanitizer Recalled for Unapproved Methanol Content

    SG24 LLC is recalling SkinGuard 24 All-Day Hand Sanitizer because it is an unapproved new drug containing methanol.

    Product
    SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump, Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147103
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1559-2020·2020-09-09

    Hand Sanitizer Recalled for Potential Methanol Contamination

    Roqueplast is recalling Command Brands GelAnti Bac hand sanitizer due to potential contamination with undeclared methanol.

    Product
    Command Brands GelAnti Bac Instant Hand Sanitizer, 70% Alcohol, , 8 FL OZ 250mL bottle, Roqueplast S.A. de C.V. Cda. Adolfo Manfredi #7 Altizapan de Zaragoza CP 52958 Edo de Mexico UPC 8 52239 00689 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1359-2020·2020-09-09

    Whole Foods Market Recalls Forteto Genovese Pesto Cheese for Undeclared Egg

    Whole Foods Market is recalling Forteto Genovese Pesto cheese nationwide due to undeclared egg whites (lysozyme). Consumers with egg allergies should not eat the product.

    Product
    Whole Foods Market IL FORTETO Genovese Pesto PLU 20017100000 Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1361-2020·2020-09-09

    Whole Foods Market Recalls Sliced Cheese for Undeclared Egg Allergen

    Whole Foods Market is recalling sliced Mitica Mahon cheese nationwide due to undeclared lysozyme from egg whites, posing a risk to individuals with egg allergies.

    Product
    Whole Foods Market Mitica Mahon PLU 29341800000 Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1573-2020·2020-09-09

    Skin Guard 24 Hand Sanitizer Recalled for Unapproved Methanol Content

    SG24 LLC is recalling Skin Guard 24 All-Day Hand Sanitizer pens because they are labeled to contain methanol, making them unapproved new drugs.

    Product
    Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147097
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1572-2020·2020-09-09

    SkinGuard 24 Hand Sanitizer Recalled for Unapproved Methanol Content

    SG24 LLC is recalling SkinGuard 24 Hand Sanitizer because it is an unapproved new drug containing methanol.

    Product
    SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump, Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147125
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1354-2020·2020-09-09

    Whole Foods Market Recalls Sliced Cheese for Undeclared Egg Allergen

    Whole Foods Market is recalling specific sliced cheeses due to undeclared lysozyme from egg whites, posing a risk to individuals with egg allergies.

    Product
    Whole Foods Market El Trigal 12 Month Old Manchego PLU 29329500000; Whole Foods Market El Trigal 6 Month Old Manchego PLU 29329900000; Whole Foods Market Mitica Cordobes PLU 29335700000; Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1356-2020·2020-09-09

    Whole Foods Market La Marquesa Herb Manchego Raw Milk Cheese Recalled for Undeclared Egg

    Whole Foods Market is recalling La Marquesa Herb Manchego Raw Milk cheese because it contains undeclared egg whites (lysozyme).

    Product
    Whole Foods Market La Marquesa Herb Manchego Raw Milk - Aged 60 days or More PLU 29399800000 Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V547000·2020-09-09

    Jayco Recalls 2019-2020 Motorhomes Due to Electrical Fire Risk

    Jayco is recalling 2019-2020 Entegra Reatta, Jayco Embark, and Entegra ReattaXL motorhomes because a damaged circuit board could increase the risk of a fire.

    Product
    ENTEGRA — ENTEGRA, JAYCO REATTA, EMBARK, REATTA XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1358-2020·2020-09-09

    Whole Foods Market Recalls Chimay Biere Cheese for Undeclared Egg

    Whole Foods Market is recalling Chimay Biere cheese due to undeclared egg whites. The product was sold nationwide with sell-by dates until September 11, 2020.

    Product
    Whole Foods Market Chimay Biere PLU 29351700000 Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V548000·2020-09-09

    Jayco Recalls Motorhomes Due to Leveling System Bracket Failure Risk

    Jayco is recalling specific 2016-2019 motorhomes because leveling system brackets may fail, causing components to contact the ground and increasing crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA GREYHAWK PRESTIGE, REDHAWK, GREYHAWK, redundant ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E065000·2020-09-09

    Horizon Global Recalls U-Haul, Draw-Tite, and Reese Towpower Trailer Hitches

    Horizon Global is recalling specific U-Haul, Draw-Tite, and Reese Towpower trailer hitches sold between November 2019 and August 2020 due to a defect that may prevent the pintle hook from locking securely.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2927-2020·2020-09-09

    Siemens Dimension Vista Troponin I Reagent Cartridge Recalled for Negative Bias

    Siemens Healthcare Diagnostics is recalling Dimension Vista High Sensitivity Troponin I reagent cartridges because they may exhibit a negative bias with patient samples.

    Product
    Dimension Vista High Sensitivity Troponin I (TNIH) Flex reagent cartridge-IVD-In vitro diagnostic use in the quantitative measurement of cardiac troponin I in human plasma Catalog Number K6427, SMN# 104471067
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20177·2020-09-09

    WHILL Recalls Model Ci Electric Vehicles Due to Control Malfunction

    WHILL is recalling about 1,160 Model Ci personal electric vehicles because a control pad malfunction can cause unintended power changes and speed fluctuations, posing crash and injury hazards.

    Product
    WHILL Personal Electric Vehicles, Model Ci
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2921-2020·2020-09-09

    Siemens Sensis Vibe Hemo System Recalled for Connector Defect

    Siemens is recalling 110 Sensis Vibe Hemo systems because a connector may break, potentially causing the device to stop functioning and lose vital signs.

    Product
    Siemens Sensis Vibe Hemo system in combination with the MicroPodTM EtCO2 module-diagnostic and administrative tool supporting hemodynamic catheterization and/or electrophysiology studies, for cardiac as well as interventional Radiology.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20178·2020-09-09

    Royal Gourmet Recalls Patio 2-Burner Gas Grills Due to Fire Hazard

    Royal Gourmet is recalling about 1,100 Patio 2-Burner Propane Gas Grills sold at Wayfair.com because the plastic regulator hose can melt and catch fire.

    Product
    Patio 2-Burner Propane Gas Grills with Side Shelves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2919-2020·2020-09-09

    Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects

    Cardinal Health is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect may cause holes and tears at the cuffs.

    Product
    PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2916-2020·2020-09-09

    Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects

    Cardinal Health 200, LLC is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect may cause holes or tears at the cuffs.

    Product
    PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2918-2020·2020-09-09

    Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects

    Cardinal Health 200, LLC is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect may cause holes and tears at the cuffs.

    Product
    PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for…
    Category
    Medical Device
    Distribution
    Distributed nationwide