Lower riskMedical device recall · FDA · Published April 11, 2025
Medical Depot iGo2 DC Car Adapter Recall: Hot Housing Risk
Medical Depot recalls iGo2 DC Car Adapters for oxygen concentrators that may overheat, deforming the housing. Affected units sold from 2023-01-01 to 2024-12-31. No remedy specified in recall.
Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
Take action
Contact the company
📍Recalling firmMedical Depot Inc.99 Seaview Blvd Fl 2 · Port Washington, NY 11050-4606
✎ GovInfoNow plain-language explainer
Medical Depot is recalling iGo2 DC Car Adapters used with portable oxygen concentrators because the power cord housing can overheat and deform. This poses a risk of burns or fire if the housing becomes too hot. The recall affects units sold between January 2023 and December 2024. Read more at govinfonow.com/recall/52461-medical-depot-igo2-dc-car-adapter-recall-hot-housing-risk.
“Medical Depot iGo2 DC Car Adapter Recall: Hot Housing Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52461-medical-depot-igo2-dc-car-adapter-recall-hot-housing-risk. Based on FDA recall #Z-1727-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1727-2025%22&limit=1).
Medical Depot Inc. recalled iGo¿2 DC Car Adapters on April 11, 2025, after the FDA announced the potential for the power cord housing to become hot and deform. The agency issued the recall for devices distributed worldwide.
How to tell if you have it
Brand: Medical Depot
Product: iGo¿2 DC Car Adapter
Catalog No.: DV6X-619
UDI: 885304020585
Cord Revision: Rev E
Lot No.: beginning with 2023-01-01 through 2024-12-31
The hazard
The FDA stated the hazard is a potential for the DC Power Supply housing to become hot to the touch and deform the plastic housing.
Context
GovInfoNow's records show Medical Depot Inc. has one other recall on record since June 14, 2024, involving a Nitro Glide Knee Walker with a risk of falling. Other recent recalls of similar products include Philips Allura Xper FD10F Medical System Recall (Dec. 15, 2025) and Medline Semi Electric Lightweight Bed Recall (Nov. 26, 2025).
How to tell if you have this one
Check for the DC Cord Code: Catalog No. DV6X-619. The adapter was sold with iGo2 Portable Oxygen Concentrator Systems from January 2023 to December 2024. Look for lot numbers starting with 2023-01-01 through 2024-12-31.
Brand
Medical Depot
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Adapter Details
Identify the catalog number (DV6X-619) and lot number range (2023-01-01 to 2024-12-31) to confirm if your adapter is affected.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Albania, Austria, Bahrain, Belgium, Bosnia and Herzegovina, Bulgaria, Canada, China, Colombia, Croatia, Cyprus, Czech Republic, France, Germany, Great Britain, Greece, Hong Kong,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 40 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1727-2025 (April 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1727-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.