Dr¿ger Perseus A500 Anesthesia Workstation — Class I medical device recall Z-1512-2024
Ongoing recall by Draeger Medical, Inc., reported 2024-04-24, distributed nationwide. Unexpected shutdown while operating on battery power.
| Recall number | Z-1512-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Draeger Medical, Inc., Telford, PA, United States |
| Recall initiated | 2024-03-20 |
| Classified | 2024-04-18 |
| Reported by FDA | 2024-04-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BE, BG, BH, BO, BR, CA, CH, CN, CR, CZ, DE, DK, EC, EG, ES, FI, FR, GB, GR, HR, HU, ID, IE, IL, IN, IQ, IR, IT, JO, JP, KE, KR, KW, LB, LT, MA, MX, MY, NL, NO, NZ, OM, PA, PE, PH, PK, PL, PT, QA, RO, RS, SA, SE, SG, SI, SK, TH, TR, TW, UA, UY, VN, ZA |
| Quantity | 16,841 units |
| UPC / GTIN / UDI-DI | 04048675253600 |
Product
Dr¿ger Perseus A500 Anesthesia Workstation
Reason for recall
Unexpected shutdown while operating on battery power.
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-1512-2024. 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.