FDA Device recall Z-1512-2024
Dr¿ger Perseus A500 Anesthesia Workstation
- FDA Device
- Class I
- ongoing
- Published 2024-04-24
On 2024-04-24 the FDA classified a Class I recall of Dr¿ger Perseus A500 Anesthesia Workstation by Draeger Medical, citing unexpected shutdown while operating on battery power.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1512-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-03-20 |
| Published | 2024-04-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Draeger Medical |
| Distribution | US |
Product
Dr¿ger Perseus A500 Anesthesia Workstation
Reason
Unexpected shutdown while operating on battery power.
Identifiers
| code_info | Material No. MX06000; UDI-DI: 04048675253600; All Serial No. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 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 - Carina Sub-Acute Care Ventilator
FDA Device · Class I · 2023-08-30 · Draeger Medical
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1512-2024%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.