FDA Device recall Z-1450-2023
VentStar Bag Set (N) 110, MP00383
- FDA Device
- Class I
- terminated
- Published 2023-05-24
On 2023-05-24 the FDA classified a Class I recall of VentStar Bag Set (N) 110, MP00383 by Draeger Medical, citing glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1450-2023 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2023-04-17 |
| Published | 2023-05-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Draeger Medical |
| Distribution | US |
Product
VentStar Bag Set (N) 110, MP00383
Reason
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Identifiers
| code_info | UDI-DI: 04048675421887; All lots. |
|---|
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-1450-2023%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.