FDA Device recall Z-1440-2014
Draeger Oxylog 3000 plus ventilators, emergency and transport ventilator
- FDA Device
- Class I
- terminated
- Published 2014-04-16
On 2014-04-16 the FDA classified a Class I recall of Draeger Oxylog 3000 plus ventilators, emergency and transport ventilator by Draeger Medical Systems, citing the potentiometers (knobs) for setting the ventilation parameters may have contact interrupted and the device discontinues ventilation, gives an audible alarm and displays the err….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1440-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-03-05 |
| Published | 2014-04-16 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Draeger Medical Systems |
| Distribution | US |
Product
Draeger Oxylog 3000 plus ventilators, emergency and transport ventilator. Part number: 5704833
Reason
The potentiometers (knobs) for setting the ventilation parameters may have contact interrupted and the device discontinues ventilation, gives an audible alarm and displays the error message Poti unplugged.
Identifiers
| code_info | Oxylog 3000 plus, Part number: 5704833 with serial numbers: ASEK-0003, ASEK-0004, ASEK-0005 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1440-2014%22
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