The Recall Desk

State

US Virgin Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38701–38725 of 73916

  • HighCPSC·18150·2018-05-08

    Hauck Recalls Nerf Battle Racer Go-Karts Due to Steering Wheel Hazards

    Hauck is recalling Nerf Battle Racer go-karts because the steering wheel can detach, break, or crack, posing laceration and collision risks to children.

    Product
    Hauck Nerf® Battle Racer go-karts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V301000·2018-05-08

    Thomas Built Buses Minotour Recalled for Wheelchair Lift Wiring Defect

    Daimler Trucks North America is recalling 2002-2018 Thomas Built Buses Minotour school buses with wheelchair lifts due to a wiring defect that allows the lift to operate while the vehicle is in motion.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V300000·2018-05-08

    Freightliner Recalls Cascadia Trucks Due to Air Bag Fastener Defect

    Daimler Trucks North America is recalling 2018-2019 Freightliner Cascadia vehicles because driver's air bag fasteners may not be installed correctly, potentially affecting deployment.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V299000·2018-05-07

    Nova Bus Recalls 2015-2017 LFS Models Due to Brake Component Defect

    Nova Bus is recalling 2015-2017 LFS and LFS Artic transit buses because a brake guide pin may break, potentially causing loss of braking ability or tire pressure.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V296000·2018-05-04

    Forest River Surveyor Recalled for Refrigerator Overheating Fire Risk

    Forest River is recalling 2018 Surveyor recreational trailers because a missing fan in the slide-out refrigerator may cause overheating and increase the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V298000·2018-05-04

    Entegra Recalls 2019 Vision and Emblem Motorhomes for Wiper Defect

    Entegra is recalling 2019 Vision and Emblem motorhomes because the windshield wiper motor may fail in heavy snow or ice, reducing driver visibility.

    Product
    ENTEGRA — ENTEGRA VISION, EMBLEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V295000·2018-05-03

    GM Recalls 2014-2017 Chevrolet Express and GMC Savana for Fire Risk

    General Motors is recalling 2014-2017 Chevrolet Express and GMC Savana vans because liquid leakage in the driver's window switch can cause corrosion and increase the risk of a fire.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V287000·2018-05-03

    Porsche Recalls 2015 918 Spyder for Rear Suspension Control Arm Defect

    Porsche is recalling 2015 918 Spyder vehicles because rear suspension connecting shafts may fail due to stress corrosion cracking, increasing the risk of a crash.

    Product
    PORSCHE — PORSCHE 918 SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V286000·2018-05-03

    Jayco Recalls 2018 Eagle Fifth Wheel Trailers Due to Pin Box Defect

    Jayco is recalling 2018 Eagle HT fifth wheel trailers because a spindle placement error in the pin box may cause the bearing to become loose, increasing the risk of a crash.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V290000·2018-05-03

    Navistar Recalls 2019 IC Bus CE School Buses Due to Brake Line Routing

    Navistar is recalling 2019 IC Bus CE school buses because an improperly routed air supply line may cause unintentional parking brake modulation, increasing crash risk.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V288000·2018-05-03

    Daimler Recalls 2017 Sprinter Vans for Missing Structural Welds

    Daimler Vans USA is recalling 2017 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vans because missing spot welds may reduce body strength in a crash.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V291000·2018-05-03

    GM Recalls 2015-2016 Chevrolet Tahoe and Silverado 1500 for Seat Belt Cable Defect

    General Motors is recalling 2015-2016 Chevrolet Tahoe and Silverado 1500 Police Pursuit and Special-Service vehicles because the driver's seat belt pretensioner cable may fatigue and break, increasing injury risk in a crash.

    Product
    CHEVROLET — CHEVROLET TAHOE, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V292000·2018-05-03

    Jayco Jay Series Trailers Recalled for Roof Lift Mechanism Defect

    Jayco is recalling 2011 and 2013 Jay Series camping trailers because misuse of the manual roof lift override may damage the mechanism, causing the roof to fall unexpectedly.

    Product
    JAYCO — JAYCO JAY SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0719-2018·2018-05-02

    Coastal Meds Recalls Hydroxocobalamin Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 1,506 vials of Hydroxocobalamin Injectable due to the presence of unknown particulate matter. The product was distributed nationwide.

    Product
    HYDROXOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1127-2018·2018-05-02

    Seabear Recalls Cold Smoked Coho Salmon Lox Due to Salt Deviations

    Seabear Company is recalling 2,080 units of Cold Smoked Wild Coho Salmon Lox due to water phase salt deviations and mislabeled storage instructions.

    Product
    Cold Smoked Wild Coho Salmon Lox , Gerard & Dominique Seafoods brand, Reduced Oxygen Packaging, Net Wt. 3 oz (85g). UPC 7 52047 92635 4. The package label of the Cold Smoked Coho Salmon bears this instructions "***KEEP REFRIGERATED AT OR BELOW 38 F***". The master case…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0699-2018·2018-05-02

    Premier Pharmacy Labs Recalls Morphine Sulfate Injection Due to Sterility Concerns

    Premier Pharmacy Labs is recalling specific lots of Morphine Sulfate Injection because routine testing of other lots detected microbial contamination risks.

    Product
    Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613. NDC 69623-129-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0726-2018·2018-05-02

    Coastal Meds Recalls Pyridoxine Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 635 vials of Pyridoxine Injectable due to the presence of unknown particulate matter.

    Product
    PYRIDOXINE Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1134-2018·2018-05-02

    Nxtgen Botanicals Maeng Da Kratom Recalled for Salmonella Risk

    NGB Corp is recalling Nxtgen Botanicals Maeng Da Kratom dietary supplements due to potential Salmonella contamination.

    Product
    Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0724-2018·2018-05-02

    Coastal Meds Recalls LIPO-PLEX Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling LIPO-PLEX Injectable-30 mL vials nationwide due to the presence of unknown particulate matter.

    Product
    LIPO-PLEX Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0700-2018·2018-05-02

    Premier Pharmacy Labs Recalls Morphine Sulfate Syringes Due to Sterility Concerns

    Premier Pharmacy Labs Inc is recalling 4,192 syringes of Morphine Sulfate 4 mg/mL PF Injection due to a lack of assurance of sterility.

    Product
    Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613. NDC 69623-127-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1532-2018·2018-05-02

    BD Vacutainer Push Button Blood Collection Set Recalled for Sterility Issues

    Becton Dickinson is recalling BD Vacutainer Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.

    Product
    BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 mm x 305 mm 21G x ¿ x 12 Catalog 367344
    Category
    Medical Device
    Distribution
    Distributed nationwide