FDA Device recall Z-2322-2024
Volara System
- FDA Device
- Class I
- ongoing
- Published 2024-07-24
On 2024-07-24 the FDA classified a Class I recall of Volara System by Baxter Healthcare, citing potential of the handset plug to disconnect from the nebulizer port on the blue ventilator adapter. The handset plug is required to ensure proper operation and ventilator gas flow.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2322-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-05-30 |
| Published | 2024-07-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Volara System. Blue Ventilator Adapter Module. Intermittent positive pressure breathing device component.
Reason
Potential of the handset plug to disconnect from the nebulizer port on the blue ventilator adapter. The handset plug is required to ensure proper operation and ventilator gas flow.
Identifiers
| code_info | Product Code: M07937; Lot numbers: 4210495, 4325617. |
|---|
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-2322-2024%22
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