The Recall Desk

State

US Virgin Islands product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25051–25075 of 73686

  • SevereNHTSA·21V328000·2021-05-10

    2021 Peterbilt Brake Chamber Defect May Increase Crash Risk

    PACCAR is recalling certain 2021 Peterbilt 348 and 579 vehicles due to brake chamber defects. Incorrectly assembled springs may cause pressure loss and increase crash risk.

    Product
    PETERBILT — PETERBILT 579, 348
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V330000·2021-05-10

    Eldorado Recalls 2017-2020 Models Due to Fuel Rail Leak Risk

    Eldorado is recalling 2017-2020 Axess, EZRM, and XHF vehicles because a sealing washer may not seat correctly, allowing the high-pressure fuel rail to leak and increasing fire risk.

    Product
    ELDORADO — ELDORADO XHF, EZRM, AXESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V331000·2021-05-10

    Kia Recalls Optima and Sorento Models for Brake Fluid Leak Fire Risk

    Kia is recalling 2013-2015 Optima and 2014-2015 Sorento vehicles because brake fluid may leak inside the Hydraulic Electronic Control Unit, creating a fire risk.

    Product
    KIA — KIA OPTIMA, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V329000·2021-05-10

    Spartan Fire Recalls 2009-2021 Metrostar and Gladiator Emergency Vehicles

    Spartan Fire is recalling 2009-2021 Metrostar and Gladiator emergency vehicles because a corroded solenoid may cause loss of water pressure, increasing injury risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE GLADIATOR, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V324000·2021-05-07

    Ford Recalls 2019 Transit Vehicles Due to Rear Axle Flange Warping

    Ford is recalling 2019 Transit T150, T250, and T350 vehicles with aluminum wheels because a warped axle flange may cause wheel studs to fracture and the wheel to detach.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V326000·2021-05-07

    Western Star 4700 and Freightliner fuel rail defect recall

    Daimler Trucks North America recalls 2018-2021 Western Star 4700 and Freightliner trucks due to fuel rail assembly defects that could leak and cause fires in certain conditions.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC, WESTERN STAR 108SD, XB CHASSIS, XC CHASSIS, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V327000·2021-05-07

    Thomas Built Buses Recalls Saf-T-Liner HDX School Buses for Fuel Leak Risk

    Daimler Trucks North America is recalling 2018-2021 Thomas Built Buses Saf-T-Liner HDX school buses because a sealing washer defect may cause high-pressure fuel leaks, increasing fire risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V325000·2021-05-07

    Airstream Globetrotter Travel Trailers Cabinet Door Adhesive Failure Recall

    Airstream is recalling 2020-2021 Globetrotter travel trailers because adhesive on overhead cabinet doors may fail, causing the doors to fall and potentially injure occupants.

    Product
    AIRSTREAM — AIRSTREAM GLOBETROTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21742·2021-05-06

    CFMOTO Recalls 2021 CFORCE 800XC ATVs Due to Crash Hazard

    CFMOTO is recalling about 2,050 2021 CFORCE 800XC ATVs because the electronic power steering can malfunction, causing loss of control and posing a crash hazard.

    Product
    2021 CFORCE 800XC All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V322000·2021-05-06

    Oshkosh Recalls 2021 S-Series Vehicles Due to Axle Detachment Risk

    Oshkosh is recalling 2021 S-Series vehicles because auxiliary axles may not be properly secured and could detach, increasing the risk of a crash.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V323000·2021-05-06

    Spartan Fire Recalls 2017-2020 Gladiator and MetroStar Vehicles for Fuel Leak

    Spartan Fire is recalling 2017-2020 Gladiator and MetroStar vehicles because a sealing washer may not seat correctly, causing a high-pressure fuel rail leak that increases fire risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0344-2021·2021-05-05

    ChloraPrep One-Step Recalled for Fungal Contamination and Package Breach

    CareFusion 213, LLC is recalling ChloraPrep One-Step applicators because fungal growth breached package integrity. The product is a sterile skin antiseptic.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0471-2021·2021-05-05

    Golden Medal Mushroom Inc. Recalls Enoki Mushrooms for Listeria

    Golden Medal Mushroom Inc. is recalling Enoki Mushrooms after Michigan state sampling detected Listeria monocytogenes.

    Product
    Enoki Mushroom Product of Korea Net Wt. 200 g/7.05 oz. UPC: 809165 582015 Clear plastic bag with green band of color across the bottom of the bag, Golden Medal Mushroom Inc., 1811 Sacramento St., Los Angeles, CA 90021 Keep Refrigerated; Cook through before eating.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0343-2021·2021-05-05

    FDA Recalls Chloraprep One-Step Antiseptic Due to Fungal Contamination

    CareFusion 213, LLC is recalling Chloraprep One-Step antiseptic applicators because fungal growth breached package integrity. The product is distributed nationwide and internationally.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0348-2021·2021-05-05

    ChloraPrep One-Step Recalled for Potential Fungal Growth and Package Breach

    CareFusion 213, LLC is recalling ChloraPrep One-Step applicators due to a lack of assurance of sterility. The product may allow fungal growth at labeled storage conditions, potentially breaching package integrity.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0352-2021·2021-05-05

    Imperial Extreme 2000 Capsules Recalled for Unapproved Active Ingredients

    S & B Story LLC is recalling Imperial Extreme 2000 Capsules because FDA analysis found unapproved ingredients tadalafil and sildenafil.

    Product
    Imperial Extreme 2000 Capsules, 2000 mg, 1 count blister cards, distributed S&B Shopper LLC. Little Ferry, NJ UPC 7 18122 04073 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0346-2021·2021-05-05

    CareFusion Recalls ChloraPrep Antiseptic Due to Fungal Contamination

    CareFusion is recalling ChloraPrep antiseptic applicators because fungal growth breached package integrity. The product is non-sterile, but the breach compromises the sterility of the applicators.

    Product
    ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Non-Sterile Solution - Hi-Lite Orange, 0.10 fl. oz. (3 ml) each, 25 applicators in carton, applicator is sterile if package is intact. CareFusion El Paso, TX 79912, NDC 054365-400-11…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0353-2021·2021-05-05

    FDA Recalls PremierZen Platinum 5000 for Unapproved Active Ingredients

    Na Na Collection is recalling PremierZen Platinum 5000 capsules because FDA analysis detected unapproved active ingredients tadalafil and/or sildenafil.

    Product
    PremierZen Platinum 5000, Packaged in paper packaging with a pill blister, 1 capsule per box, Distributed by New Premier Group Los Angeles CA 90006
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·21124·2021-05-05

    Scott Fetzer Recalls Wayne WaterBUG GLOW Pumps Due to Fire and Shock Hazards

    Scott Fetzer Consumer Brands is recalling Wayne WaterBUG GLOW pumps because water exposure can cause short circuits, posing fire, burn, and electrical shock risks.

    Product
    WAYNE WaterBUG GLOW Multi-Use Submersible Water Removal Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0345-2021·2021-05-05

    CareFusion Recalls ChloraPrep Antiseptic Applicators Due to Fungal Contamination

    CareFusion 213, LLC is recalling ChloraPrep One-Step antiseptic applicators because fungal growth breached package integrity under labeled storage conditions.

    Product
    ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Non-Sterile Solution -Clear, 0.10 fl. oz. (3ml) each, 25 applicators per carton, applicator is sterile if package is intact. CareFusion El Paso, TX 79912, NDC 054365-400-01 Cat. No.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0351-2021·2021-05-05

    Namoo Enterprise Recalls PremierZen Black 5000 Capsules for Unapproved Ingredients

    Namoo Enterprise LLC is recalling PremierZen Black 5000 capsules because FDA analysis found unapproved ingredients tadalafil and sildenafil.

    Product
    PremierZen Black 5000 capsules, 1 capsule per card/24 capsules per box, Distributed by New Premier Group Los Angeles CA 90006 UPC 7 2817542189 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0354-2021·2021-05-05

    Triple SupremeZen Gold 3500 Recalled for Unapproved Active Ingredients

    Na Na Collection is recalling Triple SupremeZen Gold 3500 capsules because FDA analysis found unapproved active ingredients tadalafil and/or sildenafil.

    Product
    Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 capsule per box, Distributed by VIEW LIFE Distributors Los Angeles CA 90005 UPC 7 15122 05089 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E042000·2021-05-05

    B&W Recalls Stainless Steel Locking Receiver Hitch Pins

    B&W Custom Truck Beds is recalling 5/8-inch stainless steel locking receiver hitch pins because the lock can be removed without a key, allowing the ball mount to detach.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide