The Recall Desk

State

US Virgin Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50251–50275 of 73995

  • ModerateFDA (Drugs)·D-0587-2016·2016-02-03

    Perrigo Recalls Children's Guaifenesin DM Liquid Due to Dosing Cup Errors

    Perrigo is recalling specific lots of Children's Guaifenesin DM Cherry liquid because the included dosing cups have incorrect dose markings.

    Product
    Guaifenesin DM Cherry liquid (guaifenesin 100 mg/5 mL and Dextromethorphan HBr 5 mg/5 mL), packaged in 4oz. bottles, co-packaged with a dosing cup in a carton and sold under the following: a) Sunmark, Children's Mucus Relief Cough, Guaifenesin 100 mg/Expectorant…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0606-2016·2016-02-03

    Pharmakon Recalls Provocholine Pre-diluted Sets Due to Stability Data Issues

    Pharmakon Pharmaceuticals is recalling Provocholine Pre-diluted Set II because stability data does not support the expiration dates. All lots expiring up to 11/17/2015 are affected.

    Product
    Provocholine Pre-diluted Set II in 0.9% Sodium Chloride, 4 mg/mL, 3 mL in 5 mL Syr, injectable packed in syringes, Rx only, PHARMAKON Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0604-2016·2016-02-03

    Pharmakon Recalls Lidocaine HCI Injectable Syringes Due to Stability Data

    Pharmakon Pharmaceuticals is recalling Lidocaine HCI 2% injectable syringes because stability data does not support the expiration dates.

    Product
    Lidocaine HCI (PF) Inj, USP 2%, injectable packed in syringes, Total dosage 100 mg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0603-2016·2016-02-03

    Pharmakon Recalls Midazolam Syringes Due to Insufficient Stability Data

    Pharmakon Pharmaceuticals is recalling 5,000 syringes of Midazolam 1 mg/mL because stability data does not support the expiration dates.

    Product
    Midazolam 1 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 2 mg/ 2mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0609-2016·2016-02-03

    Pharmakon Recalls Provocholine Pre-diluted Sets Due to Stability Data Issues

    Pharmakon Pharmaceuticals is recalling Provocholine Pre-diluted Set II because stability data does not support the expiration dates. The recall covers all lots expiring through November 17, 2015.

    Product
    Provocholine Pre-diluted Set II in 0.9% Sodium Chloride, 0.0625 mg/mL, 3 mL in 5 mL Syr, injectable packed in syringes, Rx only, PHARMAKON Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0586-2016·2016-02-03

    Perrigo Recalls Guaifenesin Liquid Due to Incorrect Dosing Cup Markings

    Perrigo Company PLC is recalling specific lots of Guaifenesin liquid because the included dosing cups have incorrect dose markings.

    Product
    Guaifenesin Grape liquid 100 mg/5 mL, packaged in 4oz. bottles, co-packaged with a dosing cup in a carton and sold under the following: a) H.E.B. Mucus Relief, Children's Guaifenesin, Expectorant, Age 4+, Grape Flavor, Gluten Free, Alcohol Free, 4 FL OZ (118 mL) Bottle, Made…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0597-2016·2016-02-03

    Pharmakon Recalls Morphine Sulfate Syringes Due to Stability Data Concerns

    Pharmakon Pharmaceuticals is recalling 475 syringes of Morphine Sulfate (PF) 0.5 mg/mL because stability data does not support the expiration dates.

    Product
    Morphine Sulfate (PF) 0.5 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 0.5 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0600-2016·2016-02-03

    Pharmakon Recalls Ketamine Syringes Due to Insufficient Stability Data

    Pharmakon Pharmaceuticals is recalling 600 syringes of Ketamine 100 mg/mL because stability data does not support the expiration dates.

    Product
    Ketamine 100 mg/mL, injectable packed in syringes, Total dosage 100 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V058000·2016-02-02

    Highland Ridge RV Recalls Travel Trailers With Underrated Safety Chains

    Highland Ridge RV is recalling 2015-2016 travel trailers because the safety chains are rated for less weight than the trailers' gross vehicle weight rating.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW ROAMER, HIGHLANDER, MESA RIDGE, JOURNEYER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16088·2016-02-02

    Dirt Devil Pet Vacuums Recalled for Electrical Shock Hazard

    Royal Appliance is recalling about 149,000 Dirt Devil Total Pet Cyclonic Upright vacuums in the U.S. because a cord prong can detach and remain in the outlet, posing an electrical shock risk.

    Product
    Dirt Devil® Total Pet Cyclonic Upright
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16082·2016-02-02

    Scubapro Recalls Galileo Luna and Sol Dive Computers Due to Screen Freezing

    Scubapro is recalling about 1,500 Galileo Luna and Sol dive computers because a short circuit can cause the screen to freeze or display inaccurate information, posing a risk of serious injury.

    Product
    Galileo Luna and Sol Dive Computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16C002000·2016-02-02

    Graco Recalls Extend2Fit Child Seats Due to Incorrect Recline Labeling

    Graco is recalling Extend2Fit convertible child seats manufactured between November 2015 and January 2016 because the recline label is affixed in the wrong location, which may lead to improper installation.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16T002000·2016-02-01

    Bridgestone Recalls Trailer Tires Due to Tread Separation Risk

    Bridgestone is recalling specific FS561 trailer tires manufactured in 2015-2016 because tread separation could cause a sudden loss of air pressure and increase crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V052000·2016-02-01

    Snake River Recalls 2015-2016 Horse Trailers Due to Axle Weld Failure

    Snake River Trailer Company is recalling 2015-2016 Horse Trailers because a weld on the rear axle may fail, causing the wheel assembly to separate and increasing crash risk.

    Product
    SNAKE RIVER — SNAKE RIVER HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V054000·2016-02-01

    GM Recalls 2015 Chevrolet Colorado and GMC Canyon for Steering Defect

    General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon trucks because a poor electrical connection may cause a loss of power steering assist, increasing crash risk.

    Product
    GMC — GMC, CHEVROLET CANYON, COLORADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V053000·2016-02-01

    Lexus Recalls RX Models Due to Knee Air Bag Weld Defect

    Toyota is recalling 2016 Lexus RX350 and RX450h vehicles because an improper weld may cause the driver's knee air bag inflator to leak gas, increasing injury risk in a crash.

    Product
    LEXUS — LEXUS RX350, RX HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V047000·2016-01-29

    Chrysler Recalls 2008-2009 Minivans and Journey for Air Bag Defect

    Chrysler is recalling 110,482 vehicles because corroded air bag control units may fail to deploy or deploy unexpectedly, increasing crash risk.

    Product
    DODGE — DODGE, CHRYSLER GRAND CARAVAN, TOWN AND COUNTRY, JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V051000·2016-01-29

    C&B Quality Trailer Works Recalls Horse Trailers Due to Axle Weld Failure

    C&B Quality Trailer Works is recalling 2015-2016 horse trailers because a weld on the rear axle may fail, causing the wheel assembly to separate and increasing crash risk.

    Product
    C&B QUALITY TRAILER WORKS — C&B QUALITY TRAILER WORKS HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide