FDA Device recall Z-1727-2025
iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems
- FDA Device
- Class I
- ongoing
- Published 2025-05-21
On 2025-05-21 the FDA classified a Class I recall of iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems by Medical Depot, citing potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1727-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-04-11 |
| Published | 2025-05-21 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medical Depot |
| Distribution | US |
Product
iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.
Reason
Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
Identifiers
| code_info | DC Cord Code Info: Catalog No. DV6X-619; UDI 885304020585; Cord Revision: Rev E; Lot No. beginning with 2023-01-01 thro…DC Cord Code Info: Catalog No. DV6X-619; UDI 885304020585; Cord Revision: Rev E; Lot No. beginning with 2023-01-01 through 2024-12-31. iGo2 Portable Oxygen Concentrator Systems Code Info: Catalog No. 125D, 125D-XB, 125D-BT, 125D-BT-XB, 125D-ARYA-XB; UDI 885304022237, 885304032250, 885304033257, 885304033240, 885304033516; Lot No. D23125001DS to D23A26121DS, D23706001DA to D23B16056DA, F23B06001DS to F25108143DS, F23313001DH to F25109259DH, F24212001DA to F25217150DA. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1727-2025%22
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