The Recall Desk

State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41051–41075 of 73919

  • HighNHTSA·17E054000·2017-09-27

    YSN Flame King RV Outdoor Cooktop Stove Recall for Fire Risk

    YSN Imports is recalling Flame King RV outdoor cooktop stoves because an internal cover can burn if the flame inverts, increasing the risk of a fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E053000·2017-09-27

    Bearing Technologies Recalls Duralast Wheel Spindles for Ford Edge

    Bearing Technologies is recalling Duralast Wheel Spindles for 2007-2010 Ford Edge vehicles because oversized studs may prevent correct wheel installation, increasing crash risk.

    Product
    FORD — FORD EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3137-2017·2017-09-27

    Medtronic Solarice Balloon Catheter Recalled for Stylette Removal Difficulties

    Medtronic is recalling Solarice Rapid Exchange Balloon Dilatation Catheters due to stylette removal difficulties. The recall covers 105,633 units distributed worldwide.

    Product
    Solarice Rapid Exchange Balloon Dilatation Catheter, a Percutaneous Transluminal Coronary Angioplasty (PTCA) Rapid Exchange System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1174-2017·2017-09-27

    Medisca Recalls Aminocaproic Acid API Due to CGMP Labeling Deviations

    Medisca, Inc. is recalling Aminocaproic Acid API lots because the product was manufactured for industrial use but labeled for pharmacy compounding.

    Product
    Aminocaproic Acid, USP (6-Aminohexanoic Acid) active pharmaceutical ingredient, packaged in a) 100 g jar (NDC 38779-0989-05, b) 1 kg jar (NDC 38779-0989-09), and 25 kg drum (NDC 38779-0989-07), Rx only, Packed by Medisca Inc., Plattsburgh, NY 12901, CAS: 60-32-1.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1166-2017·2017-09-27

    PharMEDium Recalls Fentanyl Citrate Due to Expired Diluent

    PharMEDium Services is recalling 295 bags of compounded Fentanyl Citrate because the diluent used was expired before the product's assigned expiration date.

    Product
    Fentanyl Citrate (Preservative Free) 20 mcg per mL (2,000 mcg per 100 mL) 100 mL total volume in a 100 mL LifeCare Bag in Sodium Chloride 0.9% Rx Only, Compounded by PharMEDium Services, LLC, Cleveland, MS 38732, NDC 61553-605-52
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3135-2017·2017-09-27

    Beckman Coulter Recalls AQUIOS CL Flow Cytometer Due to Software Error

    Beckman Coulter is recalling AQUIOS CL Flow Cytometer systems because a software configuration error may cause the device to draw samples from the wrong tube, resulting in incorrect laboratory values.

    Product
    AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer is intended for use as an in vitro diagnostic device for immunophenotyping.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3136-2017·2017-09-27

    Medtronic Euphora Balloon Catheter Recalled for Stylette Removal Difficulties

    Medtronic is recalling Euphora Rapid Exchange Balloon Dilatation Catheters due to stylette removal difficulties. The recall covers 69,081 units distributed in the US and worldwide.

    Product
    Euphora Rapid Exchange Balloon Dilatation Catheter, a Percutaneous Transluminal Coronary Angioplasty (PTCA) Rapid Exchange System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1165-2017·2017-09-27

    PharMEDium Recalls Fentanyl Citrate Bags Due to Expired Diluent

    PharMEDium Services is recalling 590 bags of compounded Fentanyl Citrate because the diluent used was expired before the product's assigned expiration date.

    Product
    Fentanyl Citrate (Preservative Free) 10 mcg per mL (1,000 mcg per 100 mL) 100 mL total volume in a 100 mL LifeCare Bag in Sodium Chloride 0.9% Rx Only, Compounded by PharMEDium Services, LLC, Cleveland, MS 38732, NDC 61553-112-52.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1169-2017·2017-09-27

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 321,900 Daytrana patches because the delivery system no longer meets release liner removal specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1163-2017·2017-09-27

    Pfizer Recalls Quillivant XR Methylphenidate Suspension for Dissolution Failures

    Pfizer is recalling 14,712 bottles of Quillivant XR methylphenidate extended-release oral suspension because the product failed dissolution specifications.

    Product
    Quillivant XR methylphenidate HCl, for extended-release oral suspension, 600 mg/120 mL total volume (When constituted with 105 mL of water, 25 mg/5 mL (5 mg/mL) when reconstituted, Rx Only, Distributed by Nextwave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc., New York, NY…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1164-2017·2017-09-27

    Pfizer Recalls Quillivant XR Methylphenidate Suspension Due to Dissolution Failure

    Pfizer is recalling 11,790 bottles of Quillivant XR methylphenidate extended-release oral suspension because the product failed dissolution specifications.

    Product
    Quillivant XR methylphenidate HCl, for extended-release oral suspension, 750mg/150 mL total volume (When constituted with 131 mL of water, 25 mg/5 mL (5 mg/mL) when reconstituted, Rx Only, Distributed by Nextwave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc., New York, NY…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·17233·2017-09-26

    Saber Grills Recalls Gas Grills and LP Regulators Due to Fire Hazards

    Saber Grills is recalling gas grills and LP regulators because a malfunctioning regulator can cause gas leaks and flame bursts, posing fire and burn risks.

    Product
    Gas grills and liquid propane (LP) regulators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V601000·2017-09-26

    RAM ProMaster City Recalled for Incorrect Tire Placard Information

    Chrysler is recalling 2015-2017 RAM ProMaster City vehicles because the tire placard contains incorrect weight, occupant, and pressure data, which may increase crash risk.

    Product
    RAM — RAM PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V597000·2017-09-25

    Keystone Recalls 2008-2009 Raptor RVs Due to Fire Risk

    Keystone RV Company is recalling 2008-2009 Raptor recreational vehicles because a faulty transfer switch may fail under high heat and load, increasing the risk of fire.

    Product
    KEYSTONE — KEYSTONE RAPTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V594000·2017-09-25

    Ford Recalls 2015 F-650 and F-750 Trucks for Steering Defect

    Ford is recalling 2015 F-650 and F-750 trucks because a steering component may loosen, potentially causing a loss of steering control.

    Product
    FORD — FORD F-750 SD, F-650 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V598000·2017-09-25

    Ford Recalls 2018 F-150 Raptors for Missing Roof Rivets

    Ford is recalling 2018 F-150 Raptor Super Cab trucks without moonroofs because missing roof rivets may reduce structural integrity, increasing injury risk in rollovers.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17231·2017-09-25

    Delta Recalls J is for Jeep Strollers Due to Fall Hazard

    Delta is recalling about 28,000 J is for Jeep jogging strollers because the leg bracket can break, posing a fall hazard to infants.

    Product
    J is for Jeep brand cross-country all-terrain jogging strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17232·2017-09-25

    Pro-Tec Recalls Multisport Helmets Due to Buckle Safety Failure

    Pro-Tec is recalling City Lite and Street Lite multisport helmets because the chin strap buckles fail to meet federal safety standards, posing a risk of head injury.

    Product
    Multisport helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V599000·2017-09-25

    Ford Recalls 2017 F-Series Trucks Due to Seat Belt Anchor Weld Defect

    Ford is recalling 2017 F-150, F-250, F-350, F-450, and F-550 trucks because the front passenger seat belt anchor may not be adequately welded, increasing injury risk in a crash.

    Product
    FORD — FORD F-350 SD, F-150, F-550 SD, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V592000·2017-09-22

    Mercedes-Benz Recalls 2016 Sprinter Vans for Driveshaft Fire Risk

    Daimler Vans USA is recalling 2016 Mercedes-Benz Sprinter 2500 and 3500 vehicles because a missing driveshaft catch strap could allow the driveshaft to strike the fuel tank, creating a fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide