The Recall Desk

State

US Virgin Islands product recalls

72,968 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
30
Most recent
2026-09-09

Of the 177 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 30 (17%) are Severe.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6001–6025 of 73145

  • SevereNHTSA·25V411000·2025-07-07

    Reading Truck Equipment Recalls 2021 Rail Gear HD Trucks for Weld Defects

    Reading Truck Group is recalling 2021 Rail Gear HD trucks because welds may crack, causing the front rail gear to shift and drag on the road, increasing crash risk.

    Product
    READING TRUCK EQUIPMENT — READING TRUCK EQUIPMENT RAIL GEAR TRUCKS HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V454000·2025-07-07

    Land Rover Range Rover Evoque Passenger Air Bag Deployment Defect

    Jaguar Land Rover is recalling 2020–2025 Range Rover Evoque vehicles because the passenger air bag may tear during deployment, reducing occupant protection and risking burn injury from escaping gases.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V376000·2025-07-07

    Kawasaki Ninja ZX-6R Motorcycles Engine Crankshaft Bushing Recall

    Kawasaki is recalling certain 2024–2025 Ninja ZX-6R motorcycles because the engine may lose power during operation due to crankshaft bushing seizure, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA ZX-6R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V455000·2025-07-07

    Ford vehicles recalled for low-pressure fuel pump failure risk

    Ford is recalling certain 2021–2023 Ford and Lincoln vehicles because the low-pressure fuel pump may fail, causing engine stalls while driving and increasing crash risk.

    Product
    FORD — FORD, LINCOLN BRONCO, F-250 SD, AVIATOR, F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V452000·2025-07-07

    Shyft Recalls Utilimaster Truck Bodies Due to Signal Converter Failure

    Shyft Group is recalling 2015-2025 Utilimaster Truck Body vehicles because a signal converter failure can cause brake lights and turn signals to stop working.

    Product
    UTILIMASTER — UTILIMASTER TRUCK BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V453000·2025-07-07

    2025 Polestar 3 vehicles recalled due to water-damaged electrical connectors

    Polestar is recalling certain 2025 Polestar 3 vehicles because water may damage electrical connectors between the engine bay and front bumper, which can cause loss of power steering assist and increase crash risk.

    Product
    POLESTAR — POLESTAR POLESTAR 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25368·2025-07-03

    Jeriflyer 8-inch Pool Drain Covers Recalled for Entrapment Hazard

    Jeriflyer 8-inch pool drain covers sold on Amazon do not meet federal safety standards and pose a risk of serious injury or death from entrapment. Consumers should immediately stop using affected pools and contact the seller for a refund.

    Product
    Jeriflyer 8-inch pool drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25374·2025-07-03

    509 Helmets Recalled Due to Risk of Head Injury

    509 helmets and 509 for Polaris helmets may fail to provide sufficient protection in a crash. One incident reported a helmet detachment during a crash resulting in a concussion.

    Product
    509 helmets and 509 for Polaris helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25371·2025-07-03

    Hyper Tough, Worx, and Portland Electric Chainsaws and Pole Saws Recall

    Positec is recalling about 49,000 Hyper Tough, Worx, and Portland brand electric corded chainsaws and pole saws due to a defective main switch that can fail and allow the saws to continue running, posing a laceration hazard.

    Product
    Hyper Tough, Worx and Portland Chainsaws and Pole Saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25372·2025-07-03

    SNLN Party Supply Toys Recalled for Battery Ingestion Hazard

    SNLN Party Supply Toys containing button cell batteries are being recalled because the battery compartments can be easily opened by children, posing a risk of serious injury or death if swallowed.

    Product
    SNLN Party Supply Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25369·2025-07-03

    Trane and American Standard Gas-Electric Packaged Units Recalled for Gas Leak Risk

    Trane U.S. Inc. recalls about 4,790 Gas/Electric Packaged Units because the fuel gas valve can open unexpectedly, causing a gas leak and fire hazard. No injuries have been reported.

    Product
    Trane and American Standard Gas/Electric Packaged Units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25367·2025-07-03

    DEWALT Grinder Flap Discs Recalled for Laceration Hazards

    DEWALT has recalled approximately 17,680 Elite Series 40G T27 High Density Flap Discs because the ceramic cloth abrasive flaps can detach during use, causing laceration and injury. Three reports of the flaps detaching resulted in cuts and scrapes.

    Product
    DEWALT® Grinder Flap Discs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25366·2025-07-03

    Predator 2000-Watt Power Stations Recalled for Electrical Shock Hazard

    Harbor Freight Tools is recalling about 6,500 Predator 2000-Watt Power Stations due to reversed wires in the AC outlet receptacles when in Emergency Power Supply mode, creating a shock hazard to consumers.

    Product
    Predator 2000W Power Stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V449000·2025-07-03

    Autocar Xspotter and Xpeditor brake air tank recall

    Autocar is recalling certain 2015-2022 Xspotter and Xpeditor vehicles with insufficient air in their brake system tanks. The defect can reduce brake function and increase stopping distance.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·025-2025·2025-07-02

    Kraft Heinz Recalls Oscar Mayer Turkey Bacon Due to Listeria Risk

    Kraft Heinz is recalling Oscar Mayer Turkey Bacon products nationwide due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    Kraft Heinz Foods Company — Kraft Heinz Foods Company Recalls Turkey Bacon Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0484-2025·2025-07-02

    Tirzepatide Injections recalled due to lack of sterility assurance

    Thrive Health Solutions is recalling Tirzepatide Injections 30mg/mL pre-filled syringes due to lack of assurance of sterility. The affected product was distributed nationwide.

    Product
    Tirzepatide Injections, 30mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0491-2025·2025-07-02

    Sodium Chloride Injection Recalled for Sterility Assurance Defect

    B Braun Medical Inc. is recalling 187,656 containers of 0.9% Sodium Chloride Injection USP due to potential sterility failures caused by pinholes in finger boxes during manufacturing. The defect may allow leaks and compromise the sterile nature of the intravenous medication.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1958-2025·2025-07-02

    Extended Tip Applicator 8CM distributed by Integra LifeSciences recalled nationwide

    Integra LifeSciences is recalling Extended Tip Applicator 8CM devices due to potentially out-of-specification endotoxin levels and lack of sterility assurance. The recall affects 6,216 units distributed across the US and internationally.

    Product
    Extended Tip Applicator, 8CM, Box of 5.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1904-2025·2025-07-02

    Broselow Pediatric Emergency Rainbow Tape recalled for incorrect dosing values

    SunMed Holdings is recalling Broselow Pediatric Emergency Rainbow Tape due to incorrect values printed on the tape that could lead to improper medication dosing and defibrillation in pediatric emergency care.

    Product
    Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev 2 Print Version The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0482-2025·2025-07-02

    Tirzepatide Injections Recalled for Lack of Sterility Assurance

    Thrive Health Solutions is recalling Tirzepatide Injections (10mg/mL, pre-filled syringes) distributed nationwide due to lack of assurance of sterility. Consumers should not use the affected product and contact their healthcare provider.

    Product
    Tirzepatide Injections, 10mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0478-2025·2025-07-02

    NAD+ Pre-Filled Syringes Recalled for Lack of Sterility Assurance

    Thrive Health Solutions is recalling NAD+ 100mg/mL pre-filled syringes (Lot #O-O8A01-25) distributed nationwide due to lack of assurance of sterility. Consumers should not use this product.

    Product
    Nicotinamide adenine dinucleotide (NAD+): 100mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0474-2025·2025-07-02

    Methylcobalamin Injectable Pre-filled Syringe Recalled for Sterility Concerns

    Thrive Health Solutions is recalling Methylcobalamin Injectable 10mg/mL pre-filled syringes (Lot #H228307, expiration 12/27/2025) due to lack of assurance of sterility. The affected product was distributed nationwide.

    Product
    Methylcobalamin Injectable, 10mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0485-2025·2025-07-02

    Tirzepatide/Cyanocobalamin Injectable Syringes Recalled Due to Sterility Assurance

    Thrive Health Solutions is recalling Tirzepatide/Cyanocobalamin Injectable 15mg/1mg/mL pre-filled syringes (Lot C03065F) due to lack of assurance of sterility. The product was distributed nationwide in the USA.

    Product
    Tirzepatide/Cyanocobalamin Injectable, 15mg/1mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide