The Recall Desk

State

US Virgin Islands product recalls

73,187 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
2026-09-23

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 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14176–14200 of 73364

  • HighNHTSA·23V663000·2023-09-29

    Winnebago Revel motorhomes electrical cable fire risk recall

    Winnebago is recalling certain 2020–2024 Revel motorhomes because cables near the lithium batteries may contact battery hold-down brackets, damaging the cables and causing a short circuit that increases fire risk.

    Product
    WINNEBAGO — WINNEBAGO REVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V656000·2023-09-28

    Autocar Recalls Xpeditor and Legend Vehicles for Steering Defect

    Autocar is recalling 2022-2023 Xpeditor and 2023 Legend vehicles because a steering column bolt may not be secured, risking sudden loss of steering.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V655000·2023-09-28

    Diamond C Trailers Recall 2023-2024 Models Due to Winch Failure

    Diamond C is recalling 2023-2024 FMAX, SDX, and PX trailers because the spare tire winch may loosen or fail, increasing crash risk.

    Product
    DIAMOND C TRAILERS — DIAMOND C TRAILERS SDX, FMAX, PX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23297·2023-09-28

    Solaray Liposomal Multivitamins Recalled for Non-Child-Resistant Packaging

    Nutraceutical Corporation is recalling approximately 85,300 bottles of Solaray Liposomal Multivitamins because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act, creating a poisoning risk for young children.

    Product
    Solaray Liposomal Multivitamins
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V657000·2023-09-28

    2023 Nissan Ariya Inverter Software May Cause Loss of Drive Power

    Nissan is recalling certain 2023 Ariya vehicles due to a potential inverter software defect that may cause an unexpected loss of drive power. The loss of drive power increases the risk of a crash.

    Product
    NISSAN — NISSAN ARIYA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23796·2023-09-28

    Polaris, Gravely, and Bobcat Utility Vehicles Seat Belt Bracket Defect

    About 280 Polaris Ranger, Pro XD, Gravely ATLAS, and Bobcat utility vehicles have defective passenger-side seat belt brackets that may separate from the frame, creating an injury risk. Consumers should stop using the vehicles and contact their dealer for repair.

    Product
    Model Year 2023 Polaris RANGER XP 1000 / XP 1000 Crew and RANGER 1000 / 1000 Crew, Model Year 2024 Polaris Pro XD Full-Size Diesel Crew, Model Year 2024 Gravely ATLAS JSV-3400, and Model Year 2024 Bobcat UV34XL Gas
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E071000·2023-09-28

    Firefly Recalls Multiplex HC Relay Cards Due to Fire Risk

    Firefly Integrations is recalling Multiplex HC Relay Cards because damaged relays may cause electrical short circuits, increasing the risk of a fire.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V654000·2023-09-28

    2024 RAM 2500 Rearview Camera Display Software Malfunction Recall

    Chrysler recalls 2024 RAM 2500 vehicles due to radio software that may prevent the rearview camera from displaying. Loss of rearview visibility increases crash risk.

    Product
    RAM — RAM 3500, 2500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23295·2023-09-28

    Trek Allant+ 7 Bicycles Recalled Due to Brake Hose Crash Hazard

    Trek is recalling about 7,000 Allant+ 7 bicycles with Tektro brakes because the rear brake hose can kink and break when turning the handlebars, causing loss of control and crashes. Trek has received 58 reports of riders losing control, including two minor injuries.

    Product
    Trek Allant+ 7 bicycles with Tektro brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23794·2023-09-28

    Secura Air Fryers Recalled Due to Fire and Burn Hazards

    Secura Inc. is recalling approximately 6,400 air fryers because a wire connection can overheat, posing fire and burn hazards. The company has received nine reports of units catching fire, burning, and smoking, though no injuries or property damage have been reported.

    Product
    Secura Air Fryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23296·2023-09-28

    Procter & Gamble Recalls Zevo Fly Insect Spray Over Rupture Hazard

    Procter & Gamble is recalling Zevo Fly, Gnat and Fruit Fly Flying Insect Killer3 Value Packs because the aerosol containers can rupture and leak, posing injury and laceration hazards.

    Product
    Zevo Fly, Gnat and Fruit Fly Flying Insect Killer3 Value Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23298·2023-09-28

    Rust-Oleum Fluorescent Pink Spray Paint Recalled for Impact Injury Hazard

    Rust-Oleum Professional Fluorescent Pink Inverted Marking Spray Paint cans are recalled because the spray valve assembly can detach with force, creating an impact injury hazard. The company has received five reports of detachment with paint splatter and no injuries reported.

    Product
    Rust-Oleum Professional Fluorescent Pink Inverted Marking Spray Paint cans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2528-2023·2023-09-27

    Intensive Care Ventilators Recalled Due to Capacitor Degradation Risk

    Hamilton Medical is recalling 12 intensive care ventilators (model Hamilton-MR1) due to degrading capacitors that may leak electrolyte, potentially causing ventilation interruption. The recall affects specific serial numbers across the US and Puerto Rico.

    Product
    Hamilton-MR1, REF: 161010, Intensive Care Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1174-2023·2023-09-27

    Novartis Withdraws SANDIMMUNE Oral Solution Bottles Due to Crystallization

    Novartis is recalling SANDIMMUNE Oral Solution bottles nationwide because they were found to contain crystals. Patients should contact their pharmacy or prescriber about affected bottles.

    Product
    SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue S.A.S., Huningue, France, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936, NDC 0078-0110-22.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2529-2023·2023-09-27

    Ventilator Control Board Spare Parts Recalled Due to Electrical Short-Circuit Risk

    Hamilton Medical is recalling 6 control board spare parts for ventilators due to degrading capacitors that may leak electrolyte and cause electrical short circuits, potentially interrupting ventilation.

    Product
    Hamilton C1/T1/MR1, REF: MSP161502/12, Control Board Spare part for ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2530-2023·2023-09-27

    Ventilator Spare Parts Recalled for Degrading Capacitor Risk

    Hamilton Medical is recalling ventilator spare parts (ESM Shielding Set) due to potentially degrading capacitors on the control board. These capacitors may leak electrolyte and cause a short circuit, interrupting ventilation.

    Product
    Hamilton-T1, REF: MSP161339/02, ESM Shielding Set, Spare Part for ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2525-2023·2023-09-27

    Portable Intensive Care Ventilator Recalled for Degrading Capacitor Issue

    Hamilton Medical is recalling 164 Hamilton-C1 portable ventilators due to degrading capacitors that may leak electrolyte, causing electrical short circuits that could interrupt ventilation.

    Product
    Hamilton-C1, REF: 161001, Portable Intensive Care Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2527-2023·2023-09-27

    Hamilton-T1 Ventilator Recall: Degrading Capacitors May Interrupt Ventilation

    Hamilton Medical recalls 1,216 Hamilton-T1 ventilators due to degrading capacitors on the control board that may leak electrolyte and interrupt ventilation. The recall affects units distributed nationwide in the US and Puerto Rico.

    Product
    Hamilton-T1, REF: 161009, Intensive Care and Transport Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1517-2023·2023-09-27

    Honey Roasted Sunflower Kernels Recalled for Undeclared Soy and Wheat

    Power Snacks Honey Roasted Sunflower Kernels are being recalled nationwide due to potential undeclared soy and wheat allergens from mislabeling. Approximately 88,084 units are affected.

    Product
    Power Snacks Honey Roasted Sunflower Kernels, Net Wt 1 oz; UPC 076500722025
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2602-2023·2023-09-27

    Stryker ACM System nozzle may disassemble during bone cement mixing

    The break-away femoral nozzle in Stryker's ACM System may disassemble during use, potentially leaving fragments in the surgical site and causing device failure.

    Product
    Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway Nozzle, Restrictors & Prox. Med. Press- Allows the user to mix bone cement with a constant high vacuum through the process. Catalog Number: 0306-705-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2595-2023·2023-09-27

    Medline Iris Scissors Recalled Due to Detachable Tip Protector Risk

    Medline is recalling 324,451 sterile iris scissors because the tip protector may detach, exposing a sharp point that could puncture sterile packaging and compromise instrument sterility.

    Product
    MEDLINE STERILE IRIS SCISSORS CVD/STD, REF DYNJ04049
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1521-2023·2023-09-27

    Honey Roasted Cashews Recalled for Undeclared Soy and Wheat Allergens

    Mount Franklin Foods is recalling three varieties of honey roasted cashews nationwide due to undeclared soy and wheat allergens caused by mislabeling.

    Product
    1. 7 Select Cashews Halves & Pieces Honey Roasted, Net Wt 3 oz, UPC 00052548723804 2. 7 Select Cashews Halves & Pieces Honey Roasted, Net Wt 5 oz, UPC 00052548723811 3. Circle K Honey Roasted Cashews, Net Wt 2 oz, UPC 194283102749
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1520-2023·2023-09-27

    Circle K Honey Roasted Peanuts recalled for undeclared soy and wheat allergens

    Mount Franklin Foods is recalling Circle K Honey Roasted Peanuts nationwide due to mislabeling that may result in undeclared soy and/or wheat allergens. Consumers with allergies to these substances should not consume this product.

    Product
    Circle K Honey Roasted Peanuts, Net Wt 2.5 oz, UPC 194283102596
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2597-2023·2023-09-27

    Stryker bone cement cartridge nozzles may disassemble during surgical use

    Stryker is recalling bone cement cartridges because the breakaway femoral nozzle applicator tip may disassemble or break off during use, potentially causing loss of device function and foreign material in the surgical site.

    Product
    Stryker ACM (Advanced Cement Mixing): 180-Gram Cement Cartridge with Breakaway Femoral Nozzle-Allows the user to mix bone cement with a constant high vacuum through the process Catalog Number: 0206-530-000
    Category
    Medical Device
    Distribution
    Distributed nationwide