The Recall Desk

State

US Virgin Islands product recalls

73,809 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48051–48075 of 73987

  • ModerateFDA (Drugs)·D-1053-2016·2016-07-06

    Aloe Source Recalls Topical Analgesic Products Due to Manufacturing Deviations

    The Aloe Source is voluntarily recalling specific lots of aloe SPORT liniment and eucalyptus cream due to CGMP deviations.

    Product
    aloe SPORT liniment TOPICAL ANALGESIC 8 fl oz. tube, ALOE VERA Liniment Topical Analgesic 8 fl oz. bottle, Manufactured by Coats International, Inc., the ALOE SOURCE SPORT Sport Thermogenic Eucalyptus Cream 1 fl oz. plastic bottle, Dallas, TX 75243, NDC 58826-704-08, UPC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1061-2016·2016-07-06

    Aidarex Recalls Ciprofloxacin Ophthalmic Solution Due to Unknown Impurity

    Aidarex Pharmaceuticals is recalling 599 bottles of Ciprofloxacin Ophthalmic Solution because testing revealed out-of-specification results for an unknown impurity.

    Product
    Ciprofloxacin OPTH 0.3% SOL, generic for: Ciloxan, Rx Only, 2.5 mL Bottle, Repackaged by: Aidarex Pharmaceuticals, MFG: Hi-Tech Pharmacal Co., Inc., Amityville, NY, 11701, NDC a) 33261-0910-01, b) 33261-0614-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1057-2016·2016-07-06

    KVK-Tech Recalls Benzphetamine Hydrochloride Tablets Due to Cosmetic Scuffing

    KVK-Tech, Inc. is recalling specific lots of Benzphetamine Hydrochloride Tablets due to cosmetic scuffing marks on the tablets.

    Product
    Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1059-2016·2016-07-06

    Valeant Recalls Secobarbital Sodium Capsules Due to Missing Anaphylaxis Warning

    Valeant Pharmaceuticals is recalling 958 bottles of SECONAL SODIUM capsules because the package insert is missing a warning regarding anaphylaxis.

    Product
    SECONAL SODIUM (secobarbital sodium) Capsules, USP, 100 mg, 100 Ct. Bottles, Rx Only. Distributed by: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ 08807. NDC: 0187-4220-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2051-2016·2016-07-06

    Cardiovascular Systems Recalls ViperWire Advance Peripheral Guide Wire Due to Missing Date

    Cardiovascular Systems Inc is recalling ViperWire Advance Peripheral Guide Wire because the pouch label was missing the use-by date.

    Product
    ViperWire Advance Peripheral Guide Wire, Sterilized with Ethylene Oxide, Rx Only. Part number 72023-02, Model Number VPR-GW-17. Five (5) guide wire pouches in one (1) guide wire box. For use with CSI Peripheral Orbital Atherectomy Devices (OAD), including Stealth 360 and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1058-2016·2016-07-06

    CVS Acid Controller Tablets Recalled for Impurity Specification Failure

    Dr. Reddy's is recalling CVS pharmacy Acid Controller tablets because stability testing revealed an out-of-specification impurity.

    Product
    CVS pharmacy Original Strength Acid Controller tablets, 10 mg, 30-count bottle, OTC, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, UPC 150049523
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V507000·2016-07-05

    GM Recalls 2009-2010 Chevrolet Impala for Passenger Air Bag Wiring Defect

    General Motors is recalling 2009-2010 Chevrolet Impalas because the front passenger seat frame may damage sensor wires, potentially disabling air bags or seat belt pretensioners in a crash.

    Product
    CHEVROLET — CHEVROLET IMPALA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V503000·2016-07-05

    Utility Recalls 2014-2016 Trailers Due to Spring Brake Valve Defect

    Utility Trailer Manufacturing Company is recalling 2014-2016 flatbed, refrigerated, and dry van trailers because improperly machined spring brake valves may delay braking, increasing crash risk.

    Product
    UTILITY — UTILITY FLATBED TRAILERS, REFRIGERATED TRAILERS, DRY VAN TRAILERS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V505000·2016-07-05

    VT Hackney Recalls Kidron and Hackney Trailers Due to Brake Defect

    VT Hackney is recalling 2014-2016 Kidron and Hackney trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    KIDRON — KIDRON, HACKNEY REFRIGERATED TRAILER, BEVERAGE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V506000·2016-07-05

    East Manufacturing Recalls 2014-2016 Trailers Due to Brake Valve Defect

    East Manufacturing is recalling 290 model year 2014-2016 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    EAST — EAST FLATBED, FLATBED TIPPER, FRAME DUMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V502000·2016-07-05

    GM Recalls Vehicles for Ignition Key Removal and Rollaway Risk

    General Motors is recalling specific Buick, Chevrolet, and GMC vehicles because the ignition key may be removed without the transmission in Park, creating a rollaway hazard.

    Product
    CHEVROLET — CHEVROLET, BUICK, GMC EQUINOX, REGAL, CRUZE, TERRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16C006000·2016-07-05

    Combi Coccoro Convertible Child Restraints Recalled for Crash Injury Risk

    Combi is recalling Coccoro Convertible Child Restraints because excessive force may be transmitted to the occupant in a crash if the seat is forward-facing and secured only with a lap belt.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V501000·2016-07-05

    Newmar Recalls Motorhomes Due to Exhaust Tube Fire Risk

    Newmar is recalling specific model year 1998-2015 motorhomes because a flexible exhaust tube may tear, allowing hot exhaust to contact other components and increase the risk of a fire.

    Product
    NEWMAR — NEWMAR KOUNTRY STAR, VENTANA, DUTCH STAR, ALL STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V504000·2016-07-05

    Jerr-Dan Recalls 2014-2016 HDR 1000 Wrecker Trucks Due to Control Defect

    Jerr-Dan is recalling 24 model year 2014-2016 HDR 1000 wrecker trucks because vehicle-mounted controls may remain engaged, causing unintended equipment movement and injury risk.

    Product
    JERR-DAN — JERR-DAN HDR 1000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V496000·2016-07-01

    Wilson Trailer Company Recalls 2015 CD-1080 and DWH-550 Trailers

    Wilson Trailer Company is recalling 2015 CD-1080 and DWH-550 trailers due to improperly machined spring brake valves that may delay braking, increasing the risk of the trailer rolling away.

    Product
    WILSON — WILSON CD-1080, DWH-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V499000·2016-07-01

    Mazda Recalls B-Series Trucks Due to Air Bag Inflator Rupture Risk

    Mazda is recalling 2007-2009 B-Series trucks in specific regions because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA B-SERIES TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V495000·2016-07-01

    FCA Recalls 2016 Ram Trucks Due to Transfer Case Shaft Fracture Risk

    FCA is recalling 2016 Ram 3500, 4500, and 5500 trucks because a misshapen transfer case shaft may fracture, potentially causing loss of motive power or rollaway.

    Product
    RAM — RAM 5500, 3500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V494000·2016-07-01

    Fontaine Recalls 2015-2017 Revolution Trailers Due to Brake Valve Defect

    Fontaine is recalling 2015-2017 Revolution trailers because improperly machined brake valves may delay spring brake application, increasing the risk of the trailer rolling away.

    Product
    FONTAINE — FONTAINE REVOLUTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V487000·2016-06-30

    Toyota Recalls Prius and Lexus CT Hybrid Vehicles for Air Bag Defect

    Toyota is recalling 2010-2012 Prius, Prius Plug-in Hybrid, and 2011-2012 Lexus CT Hybrid vehicles because a weld in the curtain shield air bag inflator may crack, causing parts to eject into the cabin.

    Product
    TOYOTA — TOYOTA, LEXUS PRIUS PLUG-IN HYBRID, PRIUS, CT HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V489000·2016-06-30

    Brenner Recalls 2015-2017 Liquid Tank Trailers Due to Brake Defect

    Brenner is recalling 2015-2017 Liquid Tank trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    BRENNER — BRENNER LIQUID TANK
    Category
    Vehicle
    Distribution
    Distributed nationwide