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.

50001–50025 of 73995

  • LowFDA (Devices)·Z-0851-2016·2016-03-02

    BD FMC7 FITC Recalled for Incorrect Expiration Date Labeling

    Becton, Dickinson and Company is recalling 78 units of BD FMC7 FITC reagent because the vial labels display an incorrect expiration date.

    Product
    BD FMC7 FITC: Model 430918. FMC7 is intended for in vitro diagnostic use in the identification of cells expressing FMC7 antigen. Product Usage: Analyte Specific Reagent. FMC7 is intended for in vitro diagnostic use in the identification of cells expressing FMC7 antigen.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0727-2016·2016-03-02

    Hospira Recalls Normosol-M Bags With Incorrect Expiration Date Labeling

    Hospira is recalling 10,778 bags of Normosol-M and 5% Dextrose Injection due to an incorrect expiration date printed on the primary container.

    Product
    Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection Type 1, USP, 1000 mL Single-Dose Container bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7965-09, Barcode (01) 0 030409 796509 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0840-2016·2016-03-02

    Zimmer Biomet Recalls Knee Implants Due to Packaging Adhesion Issue

    Zimmer Biomet is recalling CR Flex and LPS Flex knee prostheses because the LDPE packaging bag adheres to the polished implant surface.

    Product
    CR Flex GSF Porous Femoral LPS Flex GSF Porous Femoral LPS Flex Porous Femoral prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer various sizes This device is indicated for patients with severe knee pain and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0728-2016·2016-03-02

    Isomeric Pharmacy Recalls Triamcinolone Diacetate Injectable Suspension Due to Labeling Errors

    Isomeric Pharmacy Solution, LLC is recalling 114 vials of Triamcinolone Diacetate Injectable Suspension because some vials may have incorrect lot numbers or expiration dates.

    Product
    Triamcinolone Diacetate Injectable Suspension, 40 mg/mL, 10mL Multi-Dose Vial for Injection, Rx only, Isomeric Pharmacy Solutions, 2401 Foothill Dr., Salt Lake City, UT 84109
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V122000·2016-03-01

    Maserati Recalls Ghibli and Quattroporte Due to Floor Mat Defect

    Maserati is recalling 2014-2016 Ghibli and Quattroporte vehicles because the driver-side floor mat anchor may break, allowing the mat to trap the accelerator pedal.

    Product
    MASERATI — MASERATI GHIBLI, QUATTROPORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16111·2016-03-01

    United Pet Group Recalls Top Fin Aquarium Power Filters for Shock Hazard

    United Pet Group is recalling Top Fin power filters for aquariums because a conductor can expose consumers to electric shock. No injuries have been reported.

    Product
    Top Fin™ Power Filters for Aquariums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E016000·2016-03-01

    Carquest DOT5 Silicone Brake Fluid Recalled for Labeling Defects

    American Grease Stick Company is recalling Carquest DOT5 Silicone Brake Fluid bottles manufactured between October 2013 and September 2015 due to missing or unclear labeling required by federal safety standards.

    Product
    SERVICE BRAKES, HYDRAULIC:FLUID recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16110·2016-03-01

    Ambient Weather Radios Recalled Due to Fire Hazard

    Ambient Weather is recalling about 57,000 radios that can overheat when plugged into AC power, posing a fire hazard.

    Product
    Ambient Weather radios
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V120000·2016-02-29

    Jayco Eagle Trailers Recalled for Unprotected Solar Battery Cable Fire Risk

    Jayco is recalling 2016 Eagle fifth wheels and travel trailers because an unprotected solar battery cable may short circuit and cause a fire.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V117000·2016-02-29

    Hyundai Recalls Equus and Genesis Vehicles for Wiper Motor Defect

    Hyundai is recalling 2011-2013 Equus and 2012 Genesis vehicles because a degrading wiper motor seal can cause corrosion and loss of wiper function, increasing crash risk in bad weather.

    Product
    HYUNDAI — HYUNDAI EQUUS, GENESIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V118000·2016-02-29

    Terex Recalls 2008-2015 Aerial Devices Due to Cylinder Contact Risk

    Terex is recalling 2008-2015 aerial devices because cylinder components may contact structural parts, potentially causing platform tilting and occupant falls.

    Product
    TEREX — TEREX AERIAL DEVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V113000·2016-02-26

    Chrysler Recalls 2015-2016 Dodge Dart Vehicles for Software Defect

    Chrysler is recalling certain 2015 and 2016 Dodge Dart vehicles because a missing software backup in the powertrain control module may increase the risk of a crash.

    Product
    DODGE — DODGE DART
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V115000·2016-02-26

    Open Range Recalls 2012-2014 Trailers Due to Incorrect Weight Labels

    Open Range is recalling 2012-2014 Mesa Ridge, Roamer, and Light trailers because incorrect Gross Vehicle Weight Rating labels may lead to overloading.

    Product
    OPEN RANGE — OPEN RANGE LIGHT, ROAMER, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V109000·2016-02-25

    Honda Recalls 2014 NSS300 Scooters for Rear Brake Line Leak

    Honda is recalling 2014 NSS300 and NSS300A scooters because improperly tightened rear brake lines may leak fluid, reducing braking function and increasing crash risk.

    Product
    HONDA — HONDA NSS300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V112000·2016-02-25

    Open Range Journeyer Trailers Recalled for Underrated Safety Chains

    Open Range is recalling 2012-2015 Journeyer trailers because the safety chains are not rated high enough to support the trailer's weight if the main connection fails.

    Product
    OPEN RANGE — OPEN RANGE JOURNEYER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V110000·2016-02-25

    Ford Recalls 2016 F-150 Trucks Due to Air Bag Sensor Defect

    Ford is recalling 2016 F-150 trucks with Multi-Contour Seats because the passenger air bag sensor may misclassify adults as children, preventing air bag deployment.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V111000·2016-02-25

    Ford Recalls 2015-2016 Transit Vehicles for Rear Seat Belt Defect

    Ford is recalling 2015-2016 Transit vans because rear seat belt buckles may fail to latch if damaged by heavy objects, increasing crash injury risk.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0672-2016·2016-02-24

    Rhino 7 3000 Recalled for Undeclared Active Pharmaceutical Ingredients

    Premiere Sales Group is recalling Rhino 7 3000 bottles because they contain undeclared active pharmaceutical ingredients, desmethyl carbondenafil and dapoxetine.

    Product
    Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide