FDA Device recall Z-2018-2023
Oxylog 3000 Plus emergency and transport ventilator
- FDA Device
- Class I
- ongoing
- Published 2023-07-19
On 2023-07-19 the FDA classified a Class I recall of Oxylog 3000 Plus emergency and transport ventilator by Draeger Medical, citing draeger has become aware of instances where the device stopped working when in use when transitioning from battery to AC operation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2018-2023 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-06-12 |
| Published | 2023-07-19 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Draeger Medical |
| Distribution | US |
Product
Oxylog 3000 Plus emergency and transport ventilator
Reason
Draeger has become aware of instances where the device stopped working when in use when transitioning from battery to AC operation.
Identifiers
| code_info | Catalog No. 5704811 & 5704813; UDI-DI: 04048675398295; All Serial No. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
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FDA Device · Class I · 2024-12-25 · Draeger Medical - Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component: Not applicable
FDA Device · Class I · 2024-11-20 · Draeger Medical - Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicable
FDA Device · Class I · 2024-11-20 · Draeger Medical - Dr¿ger Perseus A500 Anesthesia Workstation
FDA Device · Class I · 2024-04-24 · Draeger Medical
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2018-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.