Class I — Medical Depot Inc.
| Recalling firm | Medical Depot, Inc DBA Drive DeVilbiss Healthcare |
|---|---|
| Registered facility | AmFab Co., LLC (the firm's only registered facility) |
| Classification | Class I |
| Status | Ongoing |
| Reason | Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing. |
| Product | iGo2 DC Car Adapter to be used with iGo2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle. |
| Quantity | 89,532 units |
| 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, Hungary, Iceland, ISRAEL, Italy, JAPAN, Kenya, Kuwait, Latvia, Libya, Lithuania, Malaysia, Maldives, Nepal, Netherlands, Norway, Oman, Philippines, Poland, Portu… |
| Initiated | 2025-04-11 |
| Classified | 2025-05-09 |
| Recall number | Z-1727-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class I recall — Medical Depot Inc. (Z-1727-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96700/
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