FDA Device recall Z-0691-2016
Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080
- FDA Device
- Class I
- terminated
- Published 2016-02-10
On 2016-02-10 the FDA classified a Class I recall of Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080 by Draeger Medical, citing drager became aware of situations where the error message "Poti unplugged" was generated causing acoustic and visual alarms, the breathing system releases pressure and the ventila….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0691-2016 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2015-12-22 |
| Published | 2016-02-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Draeger Medical |
| Distribution | US |
Product
Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and transport ventilator with pressure support.
Reason
Drager became aware of situations where the error message "Poti unplugged" was generated causing acoustic and visual alarms, the breathing system releases pressure and the ventilation function stops operating.
Identifiers
| code_info | All Oxylog 2000 plus Ventilators with the identified catalog numbers distributed between April 2007 - December 2015. |
|---|
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-0691-2016%22
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