The Recall Desk

State

US Virgin Islands product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9126–9150 of 73169

  • SevereNHTSA·24V781000·2024-10-18

    Motiv Recalls 2021-2024 E-450 School Buses Due to Wire Connection Issue

    Motiv Power Systems is recalling 2021-2024 E-450 school buses because a loose wire connection could cause a loss of drive power, increasing crash risk.

    Product
    MOTIV — MOTIV E-450 BEV CHASSIS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V778000·2024-10-18

    2024 Ford Maverick Child Seat Tether Anchor Defect Recall

    Ford is recalling 2024 Maverick vehicles because the second-row child seat tether anchors may not properly secure a child seat due to incomplete thread engagement, increasing injury risk in a crash.

    Product
    FORD — FORD MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V773000·2024-10-18

    Mack Granite trucks recalled for non-DOT-tested tires

    Mack Trucks is recalling certain 2019–2025 Granite (GR) and 2018 Granite (GU) vehicles equipped with tires that may not have been DOT tested. The untested tires may fail, increasing crash risk.

    Product
    MACK — MACK GRANITE (GR), GRANITE (GU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V776000·2024-10-18

    Forest River Recalls School Buses Due to Incorrect Child Seat Latch Bars

    Forest River is recalling 2025-2026 Collins, Magellan, and Mid Bus school buses because incorrect child seat latch bars were installed, potentially preventing proper child seat installation.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS COLLINS SCHOOL BUS, MAGELLAN SCHOOL BUS, MID BUS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V783000·2024-10-18

    Rimac Nevera Recalled for Potential Electrical Cable Fire Risk

    Rimac is recalling 2023-2024 Nevera vehicles because a low-voltage cable may not be secured properly, posing a fire risk. Owners are advised not to drive until inspected.

    Product
    RIMAC — RIMAC NEVERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V780000·2024-10-18

    Mercedes-Benz Recalls 2025 GLB Models for Tire Sidewall Damage

    Mercedes-Benz is recalling 2025 GLB 250 and GLB 35 vehicles because tire sidewall damage may cause sudden pressure loss and loss of control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250, AMG GLB35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25011·2024-10-17

    Anker Power Banks Recalled for Fire and Burn Hazards

    Anker power banks with model numbers A1642, A1647, and A1652 have been recalled because the lithium-ion battery can overheat and catch fire, causing burn injuries. The firm has received 28 reports of overheating and fires, with two burn injuries reported.

    Product
    Anker Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25015·2024-10-17

    Colsen Fire Pits Recalled for Burn Injury Risk from Flame Jetting

    Colsen-branded tabletop fire pits are being recalled due to the risk of invisible alcohol flames causing flame jetting and fire spreading. The hazard can cause serious burns in less than one second.

    Product
    Colsen-branded fire pits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25701·2024-10-17

    Arctic Cat and Tracker Off-Road Vehicles Recalled for Crash Hazard

    Textron Specialized Vehicles is recalling about 7,000 model year 2022–2024 Arctic Cat Prowler Pro and Tracker Off Road 800SX side-by-side vehicles because they can move while the digital dash displays "park," creating a rollaway crash hazard.

    Product
    Model Years 2022-2024 Arctic Cat Prowler Pro / Pro Crew and Tracker Off Road 800SX / 800SX Crew Side by Side Recreational Off Highway Vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E088000·2024-10-17

    LiveWire Recalls Two Up Seat Kits Due to Grab Strap Defect

    LiveWire is recalling Two Up Seat Kits for Mulholland motorcycles because the passenger grab strap may detach, increasing crash risk.

    Product
    SEATS:MOTORCYCLE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V772000·2024-10-17

    2025 BMW X3 front passenger air bag may not deploy properly

    BMW is recalling certain 2025 X3 xDrive30i and X3 M50i vehicles because the front passenger air bag fabric may have been damaged during transport. A damaged air bag may not inflate properly, increasing injury risk in a crash.

    Product
    BMW — BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25012·2024-10-17

    Oliva Cigars Recalls Slim Lighters Missing Child-Safety Feature

    About 60,000 promotional cigar slim lighters branded Nub, Serie V, Cain, and Oliva lack child-resistant mechanisms and pose fire and burn hazards to young children under age 5.

    Product
    Nub, Serie V, Cain, and Oliva branded Promotional Cigar Slim Lighters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0005-2025·2024-10-16

    Z-800 Infusion System Recalled for Air-in-Line Software Algorithm Defect

    Zyno Medical LLC is recalling the Z-800 Infusion System due to a defect in the air-in-line software algorithm. Approximately 34,994 units distributed nationwide are affected by this Class I FDA recall.

    Product
    Z-800 Infusion System, Model Numbers Z-800, Z-800F, Z-800W, Z-800WF; Software Version: Z-800 6.1.01 and 6-1.07z; Z-800F 4.1.02 and 4.1.08z; Z-800W 3.1.32 and 3.1.64z, Z-800WF 3.1.32 and 3.1.64z
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V770000·2024-10-16

    2025 Ford Bronco suspension defect may cause loss of steering control

    Ford is recalling 2024-2025 Bronco and 2024 Ranger vehicles because the front upper control arm ball joint fastener may not be properly tightened or installed, potentially causing loss of steering control.

    Product
    FORD — FORD RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0035-2025·2024-10-16

    Philips Patient Information Center iX Network Connectivity Issue Affects Settings Synchronization

    Philips Patient Information Center iX devices may fail to synchronize settings when network DHCP leases expire during offline operation, causing the devices to receive new IP addresses that are not recognized after reconnection.

    Product
    Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390, Software Revision 4.0.1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0050-2025·2024-10-16

    StealthStation S8 Spine Surgery Navigation System Recalled for Software Defects

    Medtronic is recalling 1,801 StealthStation S8 surgical navigation systems due to software anomalies that can flip navigation images during spine surgery and prevent warning messages for suboptimal imaging settings.

    Product
    StealthStation S8 App versions 1.3.0 and 1.3.2, (Model # 9735762) The StealthStation System, with StealthStation Spine software, is intended as an aid for precisely locating anatomical structures in either open or percutaneous neurosurgical and orthopedic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0023-2025·2024-10-16

    Knee Replacement Implant Recalled for Out-of-Spec Locking Tabs

    The FDA is recalling the Triathlon Universal TS Baseplate Size 2 knee implant due to defective locking tabs that may not properly engage with the tibial insert, potentially causing implant failure.

    Product
    Triathlon Universal TS Baseplate Size 2 - A single use sterile implantable device intended for cemented applications during primary and revision Total Knee Arthroplasty (TKA) when the Triathlon Knee System is selected for use. Catalog Number: 5521-B-200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0053-2025·2024-10-16

    Medline Sterile Laparoscopy Pack Recalled for Component Defect

    Medline recalls Sterile Laparoscopy Packs due to a manufacturing defect in the Detachable Endo Pocket component. The tube may stretch from the pouch during surgical procedures, potentially affecting tissue collection.

    Product
    Medline Sterile Laparoscopy Pack, DYNJ68187A (REF), containing the component ConMed/Unimax Detachable Endo Pocket
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0054-2025·2024-10-16

    MEDIHONEY Dressing Applicator Pouch Recalled for Sterility Concerns

    Integra LifeSciences recalls MEDIHONEY Dressing applicator pouches due to potential pinholes that may compromise sterility. The recall affects approximately 120,124 units distributed across 36 US states and internationally.

    Product
    MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing W/APPLICATOR, 1.5oz tube (Model Number 31515) and 3.5oz tube (Model Number 31535)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0034-2025·2024-10-16

    MEDLINE Digital Blood Pressure Monitor Recalled Due to Microchip Faults

    MEDLINE is recalling 7,428 Automatic Digital Blood Pressure Monitors due to a faulty microchip causing power-on failures, display issues, and overheating. Units were distributed in the US, Panama, and Jamaica.

    Product
    MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0037-2025·2024-10-16

    FDA Recalls EPIONE Device Due to Internal Component Corrosion

    Quantum Surgical recalls 2 units of the EPIONE device v1.0.2 because rust has developed on the central axis component of the Needle Guide product. These units were distributed in Florida.

    Product
    The EPIONE device v1.0.2 is a user controlled, stereotactic accessory device intended to assist in the planning and manual advancement of one or more instruments, as well as in verification of instrument position during Computed Tomography (CT) guided percutaneous procedures. Du
    Category
    Medical Device
    Distribution
    Distributed nationwide