FDA Device recall Z-2215-2016
Oxylog 3000, Disposable Pediatric Patient Circuit, Catalog Number: 5704964 The VentStar Oxylog 3000F disposable pediatric patient breathing…
- FDA Device
- Class I
- terminated
- Published 2016-08-10
On 2016-08-10 the FDA classified a Class I recall of Oxylog 3000, Disposable Pediatric Patient Circuit, Catalog Number: 5704964 The VentStar Oxylog 3000F disposable pediatric patient breathing… by Draeger Medical, citing isolated episodes of leakage at the check valve were found.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2215-2016 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2016-05-31 |
| Published | 2016-08-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Draeger Medical |
| Distribution | US |
Product
Oxylog 3000, Disposable Pediatric Patient Circuit, Catalog Number: 5704964 The VentStar Oxylog 3000F disposable pediatric patient breathing circuit is used with the Dr¿ger Oxylog 3000 and Oxylog 3000 plus Emergency Transport Ventilators.
Reason
Isolated episodes of leakage at the check valve were found
Identifiers
| code_info | Catalog Number: 5704964 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2215-2016%22
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