FDA Device recall Z-0821-2022
Compella Therapy Air Supply Unit
- FDA Device
- Class II
- terminated
- Published 2022-03-30
On 2022-03-30 the FDA classified a Class II recall of Compella Therapy Air Supply Unit by Baxter Healthcare, citing potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0821-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-02-14 |
| Published | 2022-03-30 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Compella Therapy Air Supply Unit
Reason
Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.
Identifiers
| code_info | All lots/serial numbers UDI information: Compella Therapy Air Supply Unit - 00887761013803 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0821-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.