The Recall Desk

State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57376–57400 of 74005

  • HighNHTSA·14V537000·2014-09-05

    Harley-Davidson Recalls 2014 Motorcycles Due to Clutch Master Cylinder Defect

    Harley-Davidson is recalling 105,746 model year 2014 motorcycles because a clutch master cylinder component may fail, causing the bike to creep forward.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FXSBSE, FLHTCUTG, FLHX, FLHRSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V538000·2014-09-04

    Jet Company Recalls 2014 Side Dump Trailers Due to Suspension Bolt Failure

    Jet Company is recalling 84 model year 2014 Side Dump Trailers because suspension pivot bolts may fail, potentially causing the axle to separate and increasing crash risk.

    Product
    JET COMPANY — JET COMPANY SIDE DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V529000·2014-09-04

    Chrysler Recalls 2013-2014 SRT Viper for Air Bag Deployment Defect

    Chrysler is recalling 2013-2014 SRT Vipers because inaccurate seat sensors may cause air bags to deploy at lower-than-designed velocities, increasing injury risk.

    Product
    SRT — SRT VIPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14269·2014-09-04

    Livie and Luca Recalls Children's Shoes Due to Laceration Hazard

    Livie and Luca is recalling Carta and Cotton children's shoes because a metal thread inside the liner can poke through and cut a child's foot.

    Product
    Carta and "Cotton" Children's Shoes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14270·2014-09-04

    JVC 42-Inch Flat Panel Televisions Recalled for Tip-Over Risk

    AmTRAN Video is recalling JVC 42-inch flat panel televisions because the stand neck can crack, causing the TV to tip over and pose an impact injury risk.

    Product
    JVC 42-inch flat panel televisions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V534000·2014-09-04

    Monaco Holiday Rambler Fifth Wheel Trailers Recalled for Incorrect Tire Labels

    Allied Recreation Group is recalling 2015 Monaco Holiday Rambler fifth wheel trailers because incorrect Federal Certification labels may lead to improper tire inflation and increased crash risk.

    Product
    MONACO — MONACO HOLIDAY RAMBLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1563-2014·2014-09-03

    Abrams Royal Pharmacy Recalls Non-Sterile Mineral IV Injection

    Abrams Royal Pharmacy is recalling 74 units of Mineral IV Injection found to contain Sphingomonas paucimobilis, indicating non-sterility.

    Product
    MINERAL IV Injection, compounded by Abrams Royal Pharmacy, Inc., Dallas, TX
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1564-2014·2014-09-03

    Abrams Royal Pharmacy Recalls All Unexpired Sterile Drug Products

    Abrams Royal Pharmacy is recalling all unexpired sterile drug products due to a lack of assurance of sterility. The products were distributed nationwide and to Canada.

    Product
    All Unexpired Sterile Drug Products, compounded by Abrams Royal Pharmacy Inc., Dallas, TX
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V523000·2014-09-03

    Collins and Mid Bus School Buses Recalled for Body Joint Adhesive Defect

    NHTSA is recalling 281 model year 2014 Collins and Mid Bus school buses because inadequate adhesive on interior side panel joints may fail to meet federal safety standards.

    Product
    COLLINS — COLLINS, MID BUS DE416WR, DH416, SL408, DE516WR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2399-2014·2014-09-03

    Beta Labs Recalls Phentylene Dietary Supplement Containing DMAA

    Beta Labs is recalling Phentylene capsules because they contain DMAA, a substance not permitted in dietary supplements.

    Product
    PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599822
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V527000·2014-09-03

    Western Star 4900 Trucks Recalled for Missing Anti-lock Brake Systems

    Daimler Trucks North America is recalling 2014-2015 Western Star 4900 trucks manufactured without Anti-lock Brake Systems, which increases the risk of wheel lockup and crashes.

    Product
    WESTERN STAR — WESTERN STAR 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2400-2014·2014-09-03

    Beta Labs Recalls PHEnFX Dietary Supplement Containing Unapproved DMAA

    Beta Labs is recalling 743 units of PHEnFX dietary supplements because they contain DMAA, a substance not permitted in dietary supplements.

    Product
    PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·14750·2014-09-03

    Great Innovations Recalls Ultrasonic Humidifiers Due to Fire Hazard

    Great Innovations is recalling about 70,000 Ultrasonic Clean Mist Humidifiers sold by QVC because water can enter the base and cause a fire hazard.

    Product
    Ultrasonic Clean Mist Humidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2401-2014·2014-09-03

    Beta Labs Recalls Red Vipers Supplement Containing Illegal DMAA

    Beta Labs is recalling Red Vipers dietary supplements because they contain DMAA, an ingredient not permitted in dietary supplements.

    Product
    RED VIPERS, ADVANCED FOCUS AND CONCENTRATION, HEIGHTENED ENERGY LEVELS, 75mg EPHEDRA, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559819
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1556-2014·2014-09-03

    Alkermes Recalls VIVITROL Vials Due to Dose Delivery Failure

    Alkermes is recalling 4,364 vials of VIVITROL (naltrexone) nationwide because customer complaints reported the product failed to deliver the dose.

    Product
    VIVITROL — VIVITROL (NALTREXONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2553-2014·2014-09-03

    Siemens Dimension EXL Chemistry System Recalled for Hinge Injury Risk

    Siemens is recalling 2,757 Dimension EXL Integrated Chemistry Systems because a reagent lid hinge may shift during maintenance, posing a risk of physical injury to operators.

    Product
    Siemens Dimension EXL Integrated Chemistry System in vitro diagnostic devices intended to measure a variety of analytes in human body fluids. All Serial #s of material #s: 10636929, 10636928, 10486890, 10472176, 10639337, and 10639338.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2554-2014·2014-09-03

    Curbell Medical Recalls CareSense Bed and Chair Monitors

    Curbell Medical is recalling CareSense Wireless Advanced LCD Bed and Chair Monitors because a circuit board modification disabled the alarm function.

    Product
    CURBELL MEDICAL CareSense Wireless Advanced LCD Bed and Chair Monitor, MODEL # CSM-BC400; --- COMMON/USUAL NAME: Bed Patient Monitor; CLASSIFICATION NAME: Bed Patient Monitor --- Monitor is connected to a sensor pad that monitors the patient if they attempt to arise from a…
    Category
    Medical Device
    Distribution
    Distributed nationwide