FDA Device recall Z-3252-2026
VentStar Resus Neo
- FDA Device
- Class I
- ongoing
- Published 2026-10-07
On 2026-10-07 the FDA classified a Class I recall of VentStar Resus Neo by Draeger, citing potential cracks in the hose, which could lead to leakage or the hose falling off.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3252-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2026-09-03 |
| Published | 2026-10-07 |
| Last updated | 2026-10-13 05:30 UTC |
| Company | Draeger |
| Distribution | US |
Product
VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a resuscitation module.
Reason
Potential cracks in the hose, which could lead to leakage or the hose falling off.
Identifiers
| code_info | Part Number MP00310. UDIDI: 04048675422358. All lot numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-10-13 05:30 UTC. Current status: ongoing.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3252-2026%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.