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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Device
Medical Devices/Home Healthcare

iGo2 DC Car Adapters Recalled for Overheating and Fire Risk

Agency Publication Date: May 9, 2025
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Summary

Medical Depot Inc. has recalled 89,532 units of iGo2 DC Car Adapters used with iGo2 Portable Oxygen Concentrator Systems. The DC power supply housing can become extremely hot to the touch, causing the plastic casing to melt or deform during use in a vehicle. While no injuries have been reported, this defect poses a risk of burns and potential fire.

Risk

The power cord's housing can overheat, causing the plastic to deform or melt. This creates a direct fire hazard and a risk of burn injuries to anyone who touches the adapter while it is in operation.

What You Should Do

  1. This recall affects iGo2 DC Car Adapters (Catalog No. DV6X-619) and iGo2 Portable Oxygen Concentrator Systems used to provide supplemental oxygen in vehicles.
  2. Check your device for Catalog Numbers DV6X-619, 125D, 125D-XB, 125D-BT, 125D-BT-XB, or 125D-ARYA-XB. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled car adapter immediately to avoid the risk of overheating or fire.
  4. Return the product to the place of purchase for a refund or replacement, throw it away, or contact your healthcare provider or Medical Depot Inc. for further instructions.
  5. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding this recall.

Your Remedy Options

You have 2 options:

💰Option 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
🗑️Option 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: iGo2 DC Car Adapter
Variants: Cord Revision: Rev E
Model / REF:
DV6X-619
Lot Numbers:
2023-01-01 through 2024-12-31
UDI:
885304020585

Used with iGo2 Portable Oxygen Concentrator Systems.

Product: iGo2 Portable Oxygen Concentrator Systems
Model / REF:
125D
125D-XB
125D-BT
125D-BT-XB
125D-ARYA-XB
Lot Numbers:
D23125001DS to D23A26121DS
D23706001DA to D23B16056DA
F23B06001DS to F25108143DS
F23313001DH to F25109259DH
F24212001DA to F25217150DA
UDI:
885304022237
885304032250
885304033257
885304033240
885304033516

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96700
Status: Active
Manufacturer: Medical Depot Inc.
Sold By: Authorized Medical Equipment Distributors
Manufactured In: United States
Units Affected: 89,532 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.