The Recall Desk

State

US Virgin Islands product recalls

73,100 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 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11126–11150 of 73277

  • HighNHTSA·24V388000·2024-06-03

    2024 Forest River travel trailers recalled for insufficient tire clearance

    Forest River is recalling 2024 Rainier, Stealth Evo, Salem, Vibe, and Wildwood travel trailers due to insufficient tire clearance that may cause tire damage and loss of vehicle control.

    Product
    FOREST RIVER — FOREST RIVER RAINIER, WILDWOOD, SALEM, VIBE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V389000·2024-06-03

    Host Campers Recalls Trailers Due to Cooktop Overheating Fire Risk

    Host Industries is recalling 2022-2025 Host Campers trailers because a cooktop circuit board may overheat, increasing the risk of a fire.

    Product
    HOST CAMPERS — HOST CAMPERS EVEREST, YUKON, TAHOE, MAMMOTH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V393000·2024-06-03

    Wheel hub fasteners may loosen on 2025 Western Star and Freightliner commercial trucks

    Daimler Trucks North America is recalling 2025 Western Star, Freightliner, and Thomas Built Buses vehicles. Wheel hub fasteners may loosen, causing wheel detachment and loss of vehicle control.

    Product
    FCCC — FCCC, FREIGHTLINER, THOMAS BUILT BUSES MT55G, MT55, 114SD, MT45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·24T007000·2024-06-03

    Hankook Kinergy GT Tires Recalled for Missing Identification Codes

    Hankook is recalling specific Kinergy GT tires because they lack required week and year codes, making it difficult to identify tires involved in future safety recalls.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E041000·2024-05-31

    Oshkosh Recalls Sheppard Steering Gears for S-Series Vehicles

    Oshkosh is recalling certain Sheppard Steering Gears sold as replacement parts for S-Series vehicles because incorrect assembly may cause the gear to fracture.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V380000·2024-05-31

    Range Rover transmission can shift to neutral causing loss of drive power

    Land Rover is recalling certain 2024 Range Rover and Range Rover Sport vehicles because falling transmission oil pressure can cause the clutch to shift into neutral.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V384000·2024-05-31

    Honda Fit and HR-V rearview cameras may not display on startup

    Honda is recalling certain 2018-2020 Fit and 2019-2022 HR-V vehicles, previously covered by recall 23V-046, because the rearview camera image may not display when the engine is started with a key.

    Product
    HONDA — HONDA HR-V, FIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24248·2024-05-30

    Medline Adult Bed Rails Recalled for Entrapment and Asphyxia Risk

    Medline is recalling about 1.5 million Bed Assist Bar adult bed rails because users can become entrapped between the rail and mattress, posing a risk of asphyxiation. Two deaths have been reported.

    Product
    Medline Bed Assist Bar adult bed rails
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V383000·2024-05-30

    Autocar Recalls 2023-2024 Xpeditor and Legend Trucks for Axle Defect

    Autocar is recalling 2023-2024 Xpeditor and Legend vehicles because an improperly secured axle lock nut may allow the wheel end to separate, increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V385000·2024-05-30

    Vicinity Recalls CNG Buses Due to Fuel Leak Fire Risk

    Vicinity Motor Corporation is recalling 2017 Vi33 and 2022 Vi35 buses because low-pressure CNG hoses may leak, creating a fire or explosion risk.

    Product
    VICINITY — VICINITY VI33, VI35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V381000·2024-05-30

    Toyota Tundra and Lexus LX600 engines can fail from manufacturing debris

    Toyota is recalling certain 2022-2023 Tundra and Lexus LX600 vehicles with V35A engines because manufacturing debris can contaminate the engine and cause main bearing failure, stalling the vehicle.

    Product
    TOYOTA — TOYOTA, LEXUS TUNDRA, LX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V382000·2024-05-30

    Driverge Recalls Ford T-350 Vehicles Due to Seat Recliner Defect

    Driverge is recalling 2023-2024 Ford T-350 vehicles because the seat recliner mechanism may not engage, increasing injury risk during a crash.

    Product
    DRIVERGE — DRIVERGE FORD T-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24247·2024-05-30

    ADIOS Super Vinegar Cleaner recalled for poisoning and chemical burn risk

    Compare Brands is recalling ADIOS! Super Vinegar All Natural Cleaner due to deceptive labeling that violates federal hazardous-substances rules, posing risks of poisoning and chemical burns.

    Product
    ADIOS! Super Vinegar All Natural Cleaner, 30%
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24246·2024-05-30

    Crib Bumpers Recalled Due to Suffocation Hazard and Federal Ban Violation

    About 75 padded crib bumpers sold on AliExpress are being recalled because infants can suffocate if they roll or move into a position that obstructs breathing. Padded crib bumpers are banned under federal law.

    Product
    Crib Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24249·2024-05-30

    Black & Decker Recalls CRAFTSMAN V20 Cordless Tillers for Laceration Hazard

    Black & Decker is recalling about 44,400 CRAFTSMAN V20 Cordless Tillers/Cultivators because misleading assembly instructions can cause consumers to attach the tines upside down, creating a laceration hazard. No injuries have been reported.

    Product
    CRAFTSMAN® V20 Cordless Tillers/Cultivators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1814-2024·2024-05-29

    BiPAP A30 Ventilator Recall: Risk of Therapy Interruption and Respiratory Failure

    Philips Respironics BiPAP A30 Ventilators may experience interruption or loss of therapy during a Ventilator Inoperative alarm, potentially causing severe respiratory compromise or death in vulnerable patients.

    Product
    BiPAP A30 Ventilator, Part Number 1111143 (US and OUS) OUS Only: Part Numbers 1111144 1111145 1111147 1111148 1111149 1111150 1111154 1111181 1116155 1111144L 1111144M 1111144V BR1111143 CN1111143 R1111143 R1111150 R1111181
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1813-2024·2024-05-29

    BiPAP A40 ventilators risk therapy loss during alarm condition

    BiPAP A40 ventilators may lose therapy delivery during a Ventilator Inoperative alarm, potentially causing respiratory failure or death in vulnerable patients.

    Product
    BiPAP A40 Ventilators: BiPAP A40, Part Numbers 1111169 (US and OUS) and (OUS ONLY)1111170 1111171 1111173 1111174 1111175 1111177 1116156 1111170S BR1111169 CN1111169 IT1111169 R1111169 R1111177 R1116156 ; BiPAP A40 Pro, Part Numbers (OUS Only): ARX3100S19
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E040000·2024-05-29

    Contaminated Driver Clock Springs May Deactivate Frontal Air Bags

    American Furukawa is recalling certain driver clock springs that may have been contaminated during manufacturing. This defect can cause electrical failure and prevent the driver's air bag from deploying.

    Product
    AIR BAGS:FRONTAL:DRIVER CLOCKSPRING/SPIRAL CASSETTE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1812-2024·2024-05-29

    BiPAP V30 Auto Ventilator May Interrupt Therapy During Malfunction Alarm

    Philips BiPAP V30 Auto Ventilators may interrupt or lose therapy during a Ventilator Inoperative alarm, potentially causing hypoventilation, severe oxygen depletion, or respiratory failure.

    Product
    BiPAP V30 Auto Ventilator, Part Number 1111178
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1811-2024·2024-05-29

    Optum Nimbus II Plus Infusion Pump Recall Due to Potential Failure Modes

    OptumHealth Care Solutions LLC is recalling 208 units of the Optum Nimbus II Plus ambulatory infusion pump distributed nationwide due to potential battery failure, system errors, and drug leakage.

    Product
    Optum Nimbus II Plus, Model number AAA-00170; Ambulatory Infusion Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V377000·2024-05-29

    Lion electric school bus parking brakes can release causing roll away

    Lion Electric is recalling certain 2024-2025 LionC school buses because the parking brake may malfunction and allow the lever to release without pressing the release button.

    Product
    LION — LION LIONC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1817-2024·2024-05-29

    Philips OmniLab Advanced + Ventilator May Experience Unexpected Therapy Loss

    Philips OmniLab Advanced + Ventilators may experience an alarm condition that interrupts or stops therapy delivery. This interruption may lead to inadequate breathing support, low oxygen levels, and potentially fatal respiratory failure.

    Product
    OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124 1111125 1111126 1111127 1111138 1111141 1111142 KR1111127 R1111122 R1111123 R1111124 U1111122 U1111124
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1885-2024·2024-05-29

    Scopis ENT Navigation Software Contains Visual Guidance Alignment Error

    Unreleased software in Scopis ENT surgical navigation systems causes visual guidance to display inaccurately relative to physical reference points, affecting surgical precision. Affects 705 units nationwide.

    Product
    8000-021-002, Scopis¿ ENT Software with TGS¿ with Sofware Version: NOVA 3.6.0 RC16. Scopis is a next-generation solution for navigating functional endoscopic sinus surgery (FESS) offering surgeons highly advanced image guidance and visualization capabilities in a single system. T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2097-2024·2024-05-29

    Non-Sterile Syringes Recalled for Exceeding FDA Clearance Scope

    Jiangsu Shenli Medical has recalled Medline non-sterile syringes because manufactured sizes and configurations exceed the FDA-cleared scope. No illnesses or injuries have been reported.

    Product
    Brand Name: MEDLINE Product Name: SYR CNTRL 10ML L/L GREEN Model/Catalog Number: 91879 Product Description: NON-Sterile syringes without needles for single use Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide