The Recall Desk

State

US Virgin Islands product recalls

72,913 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
30
Most recent
2026-09-09

Of the 177 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 30 (17%) are Severe.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1976–2000 of 73090

  • SevereCPSC·26477·2026-05-07

    Youth Sweatshirts with Drawstrings Recalled for Strangulation Hazard

    Allura Imports is recalling about 120 youth sweatshirts with drawstrings due to risk of strangulation. The drawstrings can catch on objects and cause serious injury or death to children.

    Product
    Youth Sweatshirts with Drawstrings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26475·2026-05-07

    Analemma Water Bottles recalled for laceration and ingestion hazards

    Analemma Water Bottles are recalled because the inner glass liner can break, posing risk of serious injury or death from laceration and ingestion. The importer has received 20 reports of the glass breaking, including one oral injury.

    Product
    Analemma Water Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V291000·2026-05-07

    Fontaine Recalls 2025-2026 Fusion Flatbed Trailers Due to Cracked Beams

    Fontaine Trailer Company is recalling 2025-2026 Fusion flatbed trailers because hydrogen contamination during galvanization may cause main beams to crack, risking load loss and crashes.

    Product
    FONTAINE — FONTAINE FUSION FLAT BED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V290000·2026-05-07

    Jeep Cherokee power transfer unit may fail and cause rollaway

    Chrysler is recalling certain 2019-2023 Jeep Cherokee vehicles because the power transfer unit may fail, which can cause a loss of drive power or vehicle rollaway.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26467·2026-05-07

    Favoto Model H-1 Bicycle Helmets Recalled for Serious Head Injury Risk

    Favoto Model H-1 bike helmets violate mandatory safety standards and may fail to protect users in a crash, posing a risk of serious head injury or death. About 2,200 units sold on Amazon from April 2022 through January 2026 are affected.

    Product
    Favoto Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V289000·2026-05-07

    GMC Yukon and Other GM Vehicles with Transfer Case Defect

    General Motors is recalling certain 2026 GMC Yukon, Sierra 1500, Yukon XL and other GM vehicles, as well as select 2015–2020 models, due to a missing component in the drivetrain transfer case that may cause wheel lockup without warning. The defect increases the risk of a crash.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SILVERADO 1500, SUBURBAN 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26469·2026-05-07

    Rublev Colours Gum Turpentine and Mineral Spirits Bottles Recalled

    Natural Pigments is recalling about 860 bottles of Rublev Colours Gum Turpentine and Mineral Spirits due to non-compliant packaging that poses a risk of serious injury or death from child poisoning.

    Product
    Rublev Colours Gum Turpentine and Mineral Spirits Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26470·2026-05-07

    Multi-Purpose Helmets Recalled for Serious Head Injury Risk

    Multi-purpose helmets sold on Temu by Foubeaka and Geniuss are recalled because they violate mandatory bicycle helmet safety standards and can fail to protect users in a crash, posing a serious risk of injury or death.

    Product
    Multi-Purpose Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26472·2026-05-07

    Justforjoyful Rainbow Wall Toys Recalled for Choking Hazard Risk

    The CPSC has recalled Justforjoyful Rainbow Wall Toys because the drumstick attached to the xylophone component has a spherical end that violates the mandatory children's toy safety standard and poses a choking hazard. About 160 units were sold on Amazon from December 2025 through March 2026.

    Product
    Justforjoyful Rainbow Wall Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26478·2026-05-07

    EVLWZL and Gunugu Mattresses Recalled for Fire Hazard Risk

    EVLWZL and Gunugu mattresses violate mandatory flammability standards and pose a risk of serious injury or death from fire. Approximately 670 units sold through Amazon, Walmart, and Wayfair from October 2025 through March 2026 are affected.

    Product
    EVLWZL and Gunugu Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26466·2026-05-07

    Battery-operated Light Up Toys Recalled for Risk of Battery Ingestion

    ZMC Group is recalling about 124,560 battery-operated light-up toys because they contain easily accessible button cell batteries that can cause serious internal injuries or death if swallowed by children. Consumers should stop using the toys immediately and contact the manufacturer for a refund.

    Product
    Various Battery-operated Light Up Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0499-2026·2026-05-06

    Optase Dry Eye Drops Recalled for Lack of Sterility Assurance

    Scope Health is recalling Optase Dry Eye Intense Drops (Glycerin 0.2%) due to lack of assurance of sterility. The product is distributed nationwide.

    Product
    OPTASE — OPTASE (GLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0491-2026·2026-05-06

    Systane Lubricant Eye Gel Recalled Due to Sterility Concerns

    Alcon Research LLC is recalling Systane Lubricant Eye Gel Night Gel (10g) distributed nationwide due to FDA inspection observations regarding lack of assurance of sterility that may impact product quality.

    Product
    SYSTANE — SYSTANE (HYPROMELLOSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V287000·2026-05-06

    Micro Bird Recalls School Buses Due to Oil Line Fire Risk

    Micro Bird is recalling 2023-2026 G5 and 2024 MB II school buses because a drive belt pulley may damage oil lines, increasing the risk of a fire.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, MB II SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1996-2026·2026-05-06

    iLet Bionic Pancreas Software Versions Recalled for Delayed CGM Readings

    Beta Bionics is recalling iLet Bionic Pancreas units with software versions 1.4.2 and 1.4.3 due to a compatibility issue with Dexcom G7 sensors that can cause delayed glucose readings and loss of automatic insulin adjustments.

    Product
    iLet Bionic Pancreas, REF: BB1001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0492-2026·2026-05-06

    GenTeal Tears Lubricant Eye Gel Recalled Due to Sterility Concerns

    Alcon Research LLC is recalling GenTeal Tears Lubricant Eye Gel nationwide due to FDA inspection observations indicating the product may lack assurance of sterility. Consumers should not use affected lots.

    Product
    GENTEAL TEARS — GENTEAL TEARS (HYPROMELLOSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1984-2026·2026-05-06

    Immy Myco DDR Trident Neutralization Buffer B Recalled for Potential Contamination

    Immuno-Mycologics, Inc. is recalling Immy Myco DDR Trident Bulk Neutralization Buffer B (60 X 30 mL, Lot F5061154) because the product may contain contaminants. The buffer is used for clinical specimen processing for Mycobacterium spp. diagnosis.

    Product
    Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens for Mycobacterium spp. diagnosis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V286000·2026-05-06

    Micro Bird Recalls G5 Transit Buses Due to Oil Line Fire Risk

    Micro Bird is recalling 2023-2025 G5 transit buses because a drive belt pulley may damage oil lines, creating a fire risk.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2039-2026·2026-05-06

    Medline Medical Convenience Kits Recalled for Non-Sterile Alcohol Prep Pads

    Medline Industries is recalling specific lots of medical convenience kits containing Webcol Large Alcohol Prep Pads because the pads were found to be non-sterile due to contamination with Paenibacillus phoenicis bacteria discovered during a sterilization audit.

    Product
    Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: Universal Central/Art Line Insertion Kit, Medline Kit SKU ART155A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0684-2026·2026-05-06

    My Mochi strawberry frozen dessert contains a foreign object

    My Mochi Strawberry flavoured Non-Dairy Frozen Dessert is being recalled after a foreign object was found inside a retail container. 1,270 cases are affected.

    Product
    My Mochi Strawberry flavored Non-Dairy Frozen Dessert; 7.5 oz; 6 pieces per container. UPC# 0-70934-99645-8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1991-2026·2026-05-06

    Depuy Synthes ATTUNE Revision Hinge Femoral Knee Component Recall

    Depuy Synthes is recalling 3 units of the ATTUNE Revision Hinge Femoral (Right, Size 5, Cemented) knee implant due to external sterile packaging adhered to internal sterile packaging, potentially compromising product sterility.

    Product
    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2005-2026·2026-05-06

    epoc BGEM BUN Test Card for epoc Blood Analysis System

    Siemens Healthcare Diagnostics is recalling epoc BGEM BUN Test Cards due to risk of inaccurate pH and carbon dioxide readings that could lead to inappropriate or missed treatment of acid-base disorders.

    Product
    epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1992-2026·2026-05-06

    Depuy Synthes ATTUNE Revision Hinge Femoral implants recalled for sterility risk

    DePuy Synthes is recalling ATTUNE Revision Hinge Femoral knee implants because external sterile packaging was found adhered to internal packaging, potentially compromising sterility.

    Product
    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2042-2026·2026-05-06

    Medline Centurion Medical Convenience Kits Recalled for Non-Sterility

    Medline Industries is recalling Centurion medical convenience kits containing Webcol Large Alcohol Prep Pads due to discovery of non-sterile product contaminated with Paenibacillus phoenicis bacteria during sterilization testing.

    Product
    Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: LATEX FREE GENERAL PURPOSE TRAY, Medline Kit SKU 75670
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2000-2026·2026-05-06

    i-STAT Blood Gas Analyzer Cartridges Recalled for Inaccurate Results

    Abbott is recalling certain i-STAT EG6+, EG7+, and G3+ blood gas cartridges that may report falsely high CO2 and falsely low pH results due to a manufacturing issue, potentially leading to unnecessary or harmful clinical interventions.

    Product
    i-STAT EG6+ cartridge; List Number: 03P77-25;
    Category
    Medical Device
    Distribution
    Distributed nationwide