The Recall Desk

State

US Virgin Islands product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26626–26650 of 73744

  • SevereNHTSA·20V791000·2020-12-17

    Ford Recalls Transit Connect and EcoSport for Air Bag Defect

    Ford is recalling 2019-2020 Transit Connect and 2020 EcoSport vehicles because air bag modules may lack first-stage booster propellant, preventing proper deployment in a crash.

    Product
    FORD — FORD TRANSIT CONNECT, ECOSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V792000·2020-12-17

    Chevrolet Silverado 1500 Front Seat Belt Brackets May Not Secure

    General Motors is recalling certain 2020 Chevrolet Silverado 1500 and other vehicles because front-row center seat belt brackets may not be properly secured to the seat frame, potentially preventing proper restraint in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 2500, SILVERADO 3500, TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V788000·2020-12-17

    2020-2021 Ford Explorer and Lincoln Aviator motor mount fastener recall

    Ford is recalling certain 2020-2021 Explorer and Lincoln Aviator vehicles because right-hand motor mount fasteners may have been incorrectly tightened and could loosen, potentially causing the axle to disconnect from the engine and loss of power.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V798000·2020-12-17

    2020 Honda Insight Recalled for DC-DC Converter Power Loss Risk

    Honda is recalling certain 2020-2021 Insight, 2020 CR-V Hybrid, and 2020 Accord Hybrid vehicles due to a DC-DC converter fault that may prevent battery recharging, potentially causing loss of drive power and increasing crash risk. Owners can receive a free software update.

    Product
    HONDA — HONDA INSIGHT, ACCORD HYBRID, CR-V HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V794000·2020-12-17

    Land Rover Recalls 2020 Range Rover Evoque for Seat Fire Hazard

    Land Rover is recalling 2020 Range Rover Evoque vehicles because the front seat material may burn too quickly in a fire, increasing injury risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-12172020-01·2020-12-17

    Country Meats Pork Snack Sticks Recalled for Undeclared Milk Allergen

    USDA FSIS issued a public health alert for Country Meats HOT BBQ Flavor Smoked Pork Snack Sticks due to misbranding and an undeclared milk allergen.

    Product
    Country Meats, LLC — FSIS Issues Public Health Alert for Ready-to-Eat Pork Snack Stick Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V790000·2020-12-17

    GM Recalls 2021 Cadillac Escalade for Seat Belt Light Visibility Issue

    General Motors is recalling 2021 Cadillac Escalade vehicles because the front passenger seat belt and airbag status lights may be invisible in daytime, increasing crash injury risk.

    Product
    CADILLAC — CADILLAC ESCALADE NA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0121-2021·2020-12-16

    Shilpa Medicare Recalls Busulfan Injection Due to Manufacturing Deviations

    Shilpa Medicare Limited is voluntarily recalling 2,064 vials of Busulfan Injection due to CGMP deviations. The recall is nationwide and the lot expired in December 2020.

    Product
    Busulfan Injection 60 mg/10 mL (6 mg/mL), For Intravenous Infusion Only, Must be diluted before use, Single Dose Vial, Sterile, Cytotoxic Agent, Rx Only, 10 mL vial, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V786000·2020-12-16

    Audi Recalls 2020 Q3 Vehicles Due to Brake Pedal Plate Defect

    Volkswagen Group of America is recalling 2020 Audi Q3 vehicles because the brake pedal plate can bend or detach, increasing crash risk.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21055·2020-12-16

    LG Energy Solution Recalls Home Batteries Due to Fire Hazard

    LG Energy Solution Michigan is recalling about 1,815 RESU 10H home batteries because they can overheat and cause fires. Consumers should contact the company for a free replacement.

    Product
    LG Chem "RESU 10H" Lithium-Ion Residential Energy Storage System
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0120-2021·2020-12-16

    Fresenius Kabi Recalls Dexmedetomidine Injection Due to Lidocaine Contamination

    Fresenius Kabi is recalling 13,525 bottles of Dexmedetomidine HCl Injection due to cross-contamination with trace amounts of lidocaine.

    Product
    Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL Single Dose Bottle, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-671-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V785000·2020-12-16

    Volkswagen Recalls 2012-2014 Beetles for Air Bag Inflator Defect

    Volkswagen is recalling 2012-2014 Beetle and Beetle Convertible vehicles because the driver's side air bag inflator may explode due to propellant degradation.

    Product
    VOLKSWAGEN — VOLKSWAGEN BEETLE CONVERTIBLE, BEETLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0126-2021·2020-12-16

    Shilpa Medicare Recalls Docetaxel Injection Due to Manufacturing Deviations

    Shilpa Medicare Limited is recalling 2,008 vials of Docetaxel Injection USP due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Docetaxel Injection USP 160 mg/8mL (20 mg/mL), For Intravenous Infusion Only, Rx Only, 8 mL Single Use Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, NDC 72485-216-08.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0125-2021·2020-12-16

    FDA Recalls Imatinib Mesylate Tablets Due to Manufacturing Deviations

    Shilpa Medicare Limited is recalling 4,166 bottles of Imatinib Mesylate 400 mg tablets nationwide due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    IMATINIB MESYLATE — IMATINIB MESYLATE (IMATINIB MESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V787000·2020-12-16

    2021 Thomas Built Saf-T-Liner C2 Electric School Bus Brake Recall

    Daimler Trucks North America is recalling 28 electric school buses where the parking brake may release unexpectedly, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0123-2021·2020-12-16

    Shilpa Medicare Recalls Azacitidine Injection Vials Due to Manufacturing Deviations

    Shilpa Medicare Limited is recalling 6,560 vials of Azacitidine for Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall is voluntary and nationwide.

    Product
    Azacitidine for Injection 100 mg/vial, For Subcutaneous and Intravenous Use Only, Rx Only, One Single Dose Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, NDC 72606-558-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0154-2021·2020-12-16

    Chef Myron's Teriyaki Sauce Recalled for Gluten-Free Mislabeling

    JMH International is recalling Chef Myron's Premium Teriyaki Sauce because it contains wheat-derived gluten despite a gluten-free claim.

    Product
    Chef Myron's Premium Teriyaki Sauce, 64 FL OZ (1.89 L), Item # 400023118, 4 bottles/case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21053·2020-12-16

    Camp Chef Recalls Portable Gas Stoves Due to Fire Hazard

    Camp Chef is recalling about 20,600 portable gas stoves because a sharp edge on an internal gas regulator part can cause gas leaks, posing a fire hazard.

    Product
    Camp Chef portable stoves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0560-2021·2020-12-16

    Medtronic Evolut PRO System Recalled for Potential Valve Leaflet Damage

    Medtronic is recalling 71,030 Evolut PRO System units worldwide due to a potential for transcatheter aortic valve leaflet damage during post-implant balloon dilatation.

    Product
    Evolut (TM) PRO System. With the following model numbers: a. EVOLUTPRO-23, Labeled as: VLV EVOLUTPRO-23 PRO COMM 29L OUS, VLV EVOLUTPRO-23 BLUE 29L COMM OUS, VLV EVOLUTPRO-23 BLUE COMM JPN, VLV EVOLUTPRO-23 BLUE 6L COMM OUS, VLV EVOLUTPRO-23 PRO COMM 29L CAN, VLV…
    Category
    Medical Device
    Distribution
    Distributed nationwide