Drug recall
Oxylog 3000 Plus emergency and transport ventilator
FDA recall event 92443 · Class I · Draeger Medical, Inc.
Key facts
| Event ID | 92443 |
|---|---|
| Recall numbers | Z-2018-2023 |
| Recalling firm | Draeger Medical, Inc. |
| Product type | Devices |
| Products | Oxylog 3000 Plus emergency and transport ventilator |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Draeger has become aware of instances where the device stopped working when in use when transitioning from battery to AC operation. |
| Initiation date | Jun 12, 2023 |
| Report date | Jul 19, 2023 |
| City | Telford |
| State | PA |
| Country | United States |
| FEI number | 2517967 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: