The Recall Desk

State

US Virgin Islands product recalls

73,495 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
39
Most recent
2026-10-14

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 39 (22%) are Severe.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24301–24325 of 73672

  • SevereNHTSA·21V516000·2021-07-08

    Dodge Challenger, Charger, and Chrysler 300 windshield bonding defect

    Chrysler recalls 21,258 model year 2020-2021 Dodge Challenger, Dodge Charger, and Chrysler 300 vehicles for windshields that may not be properly bonded and could detach in a crash. Dealers will replace the windshield urethane sealant free of charge.

    Product
    DODGE — DODGE, CHRYSLER CHALLENGER, CHARGER, 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21762·2021-07-08

    SOWTECH Espresso Machines Recalled Due to Glass Carafe Breaking Hazard

    LoHi Tech is recalling about 24,900 SOWTECH Espresso Machines (Model CM6811) because the glass carafe can break during use, posing a burn hazard. The firm has received 48 reports of breaking carafes, resulting in five burn injuries.

    Product
    SOWTECH Espresso Machines with Glass Carafes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V520000·2021-07-08

    BMW Recalls One 2019 X5 for Potential Air Bag Deployment Failure

    BMW is recalling one 2019 X5 xDrive 40i because a manufacturing defect in the instrument panel may prevent the passenger air bag from deploying properly in a crash.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V521000·2021-07-08

    BMW Recalls 2018-2019 X3 and X4 Models Due to Air Bag Defect

    BMW is recalling 2018-2019 X3 and X4 vehicles because the front passenger air bag may fail to deploy due to a sensor assembly error.

    Product
    BMW — BMW X4, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V518000·2021-07-08

    Maintainer Service Bodies Recalled for Short Crane Mounting Bolts

    Maintainer is recalling 2019-2020 Service/Mechanics Bodies mounted on International MV607 vehicles because crane mounting bolts are too short to securely attach the crane.

    Product
    MAINTAINER — MAINTAINER SERVICE/MECHANICS BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V522000·2021-07-08

    Recreational Vehicles Recalled for Thor Motor Coach Window Vent Failure

    Thor Motor Coach is recalling multiple RV models due to defective adhesive bonding in Hehr 6400 series windows. The vented portion may detach, increasing risk of crash or injury.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY, VENETIAN, ARIA, PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V517000·2021-07-08

    2022 Chevrolet Bolt EV and Bolt EUV recalled for driver air bag fastener issue

    General Motors is recalling certain 2022 Chevrolet Bolt EV and Bolt EUV vehicles because driver-side air bag fasteners may be missing or improperly tightened. This could prevent the air bag from deploying properly in a crash.

    Product
    CHEVROLET — CHEVROLET BOLT EV, BOLT EUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V519000·2021-07-08

    2022 KIA K5 Fuel Pipe Leak Increases Fire Risk

    Kia is recalling 2022 K5 vehicles with 2.5L turbocharged engines due to fuel leaks that increase fire risk. Dealers will repair the fuel pipe at no cost.

    Product
    KIA — KIA K5, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·21760·2021-07-08

    ECHO EGi-2300 Watt Generators Recalled for Fire and Burn Hazard

    ECHO EGi-2300 Watt Generators can overheat and catch fire, posing a fire and burn hazard. The manufacturer has received four reports of overheating or fire, though no injuries have been reported.

    Product
    ECHO EGi-2300 Watt Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0641-2021·2021-07-07

    Premium OrgaZEN 7000 Capsules Recalled for Undeclared Sildenafil and Tadalafil

    Premium OrgaZEN 7000 capsules distributed nationwide have been recalled because they were marketed without FDA approval and contain undeclared sildenafil and/or tadalafil, prescription drugs that pose serious health risks.

    Product
    Premium OrgaZEN 7000 capsule, 1-count per blister card, distributed by: Nutra Vita Co, Santa Fe Springs, CA, Made in USA , UPC 0 40232 32555 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0642-2021·2021-07-07

    Ginseng Power 5000 Capsules Recalled for Undeclared Prescription Drug Ingredients

    NSNY Distributor Inc is recalling Ginseng Power 5000 capsules nationwide because they contain undeclared sildenafil and/or tadalafil, prescription medications not listed on the label or approved for sale in this product.

    Product
    Ginseng Power 5000 capsule, 1- count per blister card, GS Natural Co, Los Angeles, CA 90010, UPC 0 40232 18144 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1952-2021·2021-07-07

    LeadCare II Blood Lead Test Kit Control Test Inaccuracy Recall

    The LeadCare II Blood Lead Test Kit may generate artificially low control test results, causing blood lead levels to be underestimated in patient samples. Kits were distributed worldwide.

    Product
    LeadCare II Blood Lead Test Kit Catalog Number 70-6762
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0646-2021·2021-07-07

    ProtectoRx Ethyl Alcohol 70% Hand Sanitizer Recalled for Methanol Contamination

    ProtectoRx hand sanitizer (ethyl alcohol 70%) is being recalled nationwide because some lots were found to contain methanol and all lots were manufactured under the same conditions as the contaminated product.

    Product
    ProtectoRx (ethyl alcohol 70%), packaged in a) 2 FL OZ (59 mL), NDC 75408-002-01 and b) 16 FL OZ (473.2 mL), NDC 75408-002-02 bottles, Imported by: Dibar Labs, LLC., Sugar Land, TX 77479; Distributed by: PR Trading LLC, PO Box 19647, San Juan, PR 00910, Made in Mexico.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0645-2021·2021-07-07

    DiBAR LABS Hand Sanitizer Recalled for Methanol Contamination

    DiBAR LABS Hand Sanitizer (70% ethyl alcohol) in 16 FL OZ and 8 FL OZ bottles is being recalled nationwide because other lots and products made under the same conditions were found to contain methanol.

    Product
    DiBAR LABS Hand Sanitizer, (ethyl alcohol 70%), packaged as a) 16 FL OZ (473.1 mL) bottle, NDC 73009-001-16, UPC 8 53090 00302 0 and b) 8 FL OZ (236.5 mL) bottle, NDC 73009-0001-08, UPC 8 53090 00301 3; Distributed by: S.E.N.D, LLC., Anthony, NM 88021; Imported by: Dibar Labs…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0647-2021·2021-07-07

    Advance Hand Sanitizer Recalled for Methanol Contamination

    Dibar Labs is recalling Advance Hand Sanitizer (70% ethyl alcohol, 16 FL OZ) distributed nationwide because it was manufactured under the same conditions as lots found to contain methanol.

    Product
    ADVANCE HAND SANITIZER, (ethyl alcohol 70%), 16 FL OZ (473.2 mL), Imported by: Dibar Labs, LLC,.Sugar Land, TX 77479, Distributed by: Lifetime Health Services, Pharr, TX 78577, Made in Mexico, NDC; 79284-005-00. UPC 8 60004 06470 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1953-2021·2021-07-07

    Blood Lead Test Kit Recalled for Inaccurate Control Test Results

    Magellan Diagnostics recalls LeadCare Plus Blood Lead Test Kit after control tests generated low results, potentially underestimating patient blood lead levels. Affected lot numbers include 2011MU, 2104MU, and 2108MU.

    Product
    LeadCare Plus Blood Lead Test Kit Catalog Number 82-0004
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0644-2021·2021-07-07

    DiBAR LABS Hand Sanitizer Recalled for Methanol Contamination

    DiBAR LABS Hand Sanitizer (ethyl alcohol 70%, 8 FL OZ) is being recalled because FDA testing found three lots contain methanol contamination and have ethanol content below the label claim.

    Product
    DiBAR LABS Hand Sanitizer (ethyl alcohol 70%), 8 FL OZ. (236.5 mL), Distributed by S.E.N.D. LLC, Anthony, NM 88021, Imported by Dibar Labs, LLC, Sugar Land, TX 77479, Made in Mexico,77479, NDC 73009-0001-08 UPC 8 53090 00301 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1928-2021·2021-07-07

    Quidel Lyra SARS-CoV-2 Assay Kits Recalled for Potential False Negatives

    Quidel Corporation is recalling approximately 29,787 kits of the Lyra SARS-CoV-2 Assay due to a theoretical risk that samples with very high viral loads could produce false negative results. No false negatives have been formally reported.

    Product
    Lyra SARS-CoV-2 Assay (M120) in vitro diagnostic test reagent
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1954-2021·2021-07-07

    LeadCare Ultra Blood Lead Test Kit Recalled for Control Test Inaccuracy

    Magellan Diagnostics is recalling the LeadCare Ultra Blood Lead Test Kit due to control test failures causing potential underestimation of blood lead levels in patient samples. The recall involves 441 kits with worldwide distribution.

    Product
    LeadCare Ultra Blood Lead Test Kit Catalog Number 70-8098
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V513000·2021-07-07

    2021 Mercedes-Benz Sprinter and Freightliner Vehicles Recalled for Seat Belt Defect

    Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter, Metris, and Freightliner Sprinter vehicles because seat belt retractors may deactivate early, preventing child restraints from securing properly.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1993-2021·2021-07-07

    Percutaneous Dilation Tracheostomy Kit Recalled for Incorrect Size Labeling

    One lot of PORTEX ULTRperc Percutaneous Dilation Tracheostomy Kit (Lot 4072715) was incorrectly labeled as 7.0mm when it is 9.0mm. The 40 units were distributed in Pennsylvania, Michigan, Maryland, and Florida.

    Product
    PORTEX UNLTRperc Percutaneous Dilation Tracheostomy Kit, REF 100/596/090 - Product Usage: intended for use in a controlled setting such as an Intensive Care Unit or operating room with the assistance of trained personnel.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1982-2021·2021-07-07

    Monitor Bracket Assembly Fall Hazard Recall Affects Multiple CT Systems

    Philips is recalling 1,301 monitor bracket assemblies used with CT systems due to shaft wear that could cause monitors to fall, potentially injuring patients, operators, bystanders, or service personnel.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and PET/CT systems. Brilliance 64, Brilliance 40, Ingenuity Flex 728235 - Brilliance 40 728231/728232 - Brilliance 64 728317/728318 - Ingenuity Flex
    Category
    Medical Device
    Distribution
    Distributed nationwide