The Recall Desk

State

US Virgin Islands product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26701–26725 of 73744

  • HighNHTSA·20V777000·2020-12-11

    Altec Recalls 2020 Aerial Devices Due to Boom Valve Defect

    Altec is recalling 2020 AN67-E100 aerial devices because a shuttle cartridge was installed instead of a plug, risking unintended boom movement and injury.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V770000·2020-12-10

    Honda and Acura Recall Vehicles for Potential Drive Shaft Breakage

    Honda is recalling specific 2007-2015 Acura and Honda models because improperly coated drive shafts may break, causing loss of power or vehicle roll-away.

    Product
    ACURA — ACURA, HONDA ILX, CIVIC HYBRID, FIT, ILX HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V767000·2020-12-10

    2020-2021 Forest River XLR Toy Hauler Weight Label Defect Recall

    Forest River is recalling certain 2020-2021 XLR Boost Toy Hauler recreational vehicles with inaccurate Federal Placards that may understate the vehicle's weight, risking tire damage and crashes from overloading.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V765000·2020-12-10

    Altec Recalls 2018-2020 Digger Derricks Due to Hydraulic Valve Defect

    Altec is recalling 2018-2020 digger derricks and aerial devices because a hydraulic check valve snap ring can fail, causing unintended boom movement.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V769000·2020-12-10

    Honda Recalls 2013-2015 Accord Vehicles for Drive Shaft Defect

    Honda is recalling 2013-2015 Accord vehicles with 4-cylinder engines and CVTs in 23 states and D.C. because a lubricant issue may cause drive shafts to break, risking loss of power or vehicle roll-away.

    Product
    HONDA — HONDA ACCORD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21713·2020-12-10

    Thermo Tents Recalls Mór Series Tents Due to Fire Hazard

    Thermo Tents is recalling Mór Series tents because they are incorrectly labeled as fire retardant, posing a fire hazard.

    Product
    Crua Tri, Crua Loj, and Crua Cottage tents in the Mór Series
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21712·2020-12-10

    Scentsy Recalls Electrical Oil Warmers Due to Fire Hazard

    Scentsy is recalling Luminary Jack and Bless This Home electrical oil warmers because corrosion of electrical components poses a fire hazard.

    Product
    Scentsy Luminary Jack Warmer and Scentsy Bless This Home Warmer
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V766000·2020-12-10

    Subaru Recalls 2020 Outback and Legacy for Rearview Display Issues

    Subaru is recalling 2020 Outback and Legacy vehicles because a software update may cause the rearview display to shut off intermittently, increasing crash risk.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21714·2020-12-10

    Homfa Cabinets Recalled Due to Tip-Over and Entrapment Hazards

    Homfa HPB-087 and HPB-106 cabinets are recalled because they can tip over or entrap children if not anchored to the wall.

    Product
    Homfa HPB-087 and HPB-106 Cabinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V771000·2020-12-10

    Honda Recalls Accord and Insight Vehicles for Software Error

    Honda is recalling 2018-2020 Accord and 2019-2020 Insight vehicles because a software error may cause system malfunctions that increase crash risk.

    Product
    HONDA — HONDA ACCORD HYBRID, ACCORD, INSIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0118-2021·2020-12-09

    MPM Medical Recalls REGENECARE HA Topical Anesthetic Due to Bacteria

    MPM Medical LLC is recalling REGENECARE HA topical anesthetic hydrogel because it was found to be contaminated with Burkholderia cepacia bacteria.

    Product
    REGENECARE HA — REGENECARE HA (LIDOCAINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0514-2021·2020-12-09

    Invacare PerfectO2 V Oxygen Concentrator Recalled for Fire and Explosion Risk

    Invacare is recalling 384,767 PerfectO2 V oxygen concentrators worldwide due to a defect that may cause self-extinguishing fires or cap explosions.

    Product
    Invacare PerfectO2 V Oxygen Concentrator- intended for patients with respiratory disorders requiring supplemental oxygen Model Numbers: IRC5PO2V (US), IRC5PO2VC (Canada), All World: IRC5PO2VAW, IRC5PO2VAWL2, IRC5PO2VAWL3, IRC5PO2VAWL4, IRC5PO2VAWL5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0526-2021·2020-12-09

    CME America Recalls NeoThrive Syringe Pumps Due to Motor Wear

    CME America is recalling 4,182 NeoThrive syringe pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may damage hardware.

    Product
    CME America T-Syringe Pump - NeoThrive - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0518-2021·2020-12-09

    Medtronic MiniMed 640G Insulin Pump Recalled for Missing Solder Battery Connection

    Medtronic is recalling MiniMed 640G insulin pumps because a missing solder battery connection could interrupt power. The recall covers specific serial numbers distributed in the U.S. and abroad.

    Product
    MiniMed 640G, insulin pump, Ref/Model # MMT-1711K, MMT-1752K, MMT-1752, Rx Only - Product Usage: indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V760000·2020-12-09

    Audi Recalls 2018-2019 RS 5 Coupe for Battery Terminal Cover Defect

    Audi is recalling 2,355 2018-2019 RS 5 Coupe vehicles because an incorrect positive battery terminal cover could prevent doors from opening or hazard lights from working after a rear crash.

    Product
    AUDI — AUDI RS 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0527-2021·2020-12-09

    CME America T-Syringe Pump Recall for Motor Wear and Fluid Damage

    CME America is recalling T34L PCA syringe pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may damage hardware.

    Product
    CME America T-Syringe Pump - T34L PCA - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0516-2021·2020-12-09

    Medtronic MiniMed 670G Insulin Pumps Recalled for Battery Connection Defect

    Medtronic is recalling 391 MiniMed 670G insulin pumps because a missing solder battery connection could interrupt power to the device.

    Product
    MiniMed 670G, insulin pump, Ref/Model # MMT-1760KPK, MMT-1762KCN, MMT-1762WWK - Product Usage: indicated for continuous or periodic monitoring of glucose levels in the fluid under the skin, and detecting possible low and high glucose episodes. When using a sensor and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·21046·2020-12-09

    L G Sourcing Recalls Electric Fireplaces Due to Fire Hazard

    L G Sourcing is recalling allen + roth 62-inch electric fireplaces sold at Lowe's because wiring connectors can overheat, posing a fire hazard.

    Product
    allen + roth 62-inch Electric Fireplaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0505-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions

    Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.

    Product
    Olympus Ultrasound Endoscope, Model number: GF-UC160P-OL5 - Product Usage: used for diagnostic ultrasound imaging or fluid flow analysis of the human body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0501-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions

    Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.

    Product
    Olympus Ultrasound Endoscope, Model number :GF-UM20 - Product Usage: used with other supporting equipment for endoscopic real-time ultrasound imaging and endoscopic surgery within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0531-2021·2020-12-09

    Verathon BladderScan Prime Plus Probe Recall for Handle Cracking Risk

    Verathon is recalling 398 BladderScan Prime Plus Probes because a change in handle material and process may cause the handle to crack.

    Product
    BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the bladder noninvasively.
    Category
    Medical Device
    Distribution
    Distributed nationwide