Draeger Oxylog 3000 plus ventilators — Class I medical device recall Z-1440-2014
Terminated recall by Draeger Medical Systems, Inc., reported 2014-04-16, distributed nationwide. The potentiometers (knobs) for setting the ventilation parameters may have contact interrupted and the device
| Recall number | Z-1440-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Draeger Medical Systems, Inc., Telford, PA, United States |
| Recall initiated | 2014-03-05 |
| Classified | 2014-04-10 |
| Reported by FDA | 2014-04-16 |
| Terminated | 2014-10-31 |
| Distributed | Nationwide (US) |
| Quantity | 3 |
| Serial numbers | ASEK-0003, ASEK-0004, ASEK-0005 |
| Model numbers | 5704833 |
Product
Draeger Oxylog 3000 plus ventilators, emergency and transport ventilator. Part number: 5704833
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1440-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.