Achieva 3 — Class II medical device recall Z-1839-2024
Ongoing recall by Philips North America Llc, reported 2024-05-29, distributed nationwide. The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may
| Recall number | Z-1839-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America Llc, Cambridge, MA, United States |
| Recall initiated | 2024-05-03 |
| Classified | 2024-05-17 |
| Reported by FDA | 2024-05-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, CA, CH, CN, CZ, DE, DK, ES, FI, FR, GB, GR, HR, IT, JP, LB, LT, NL, NO, PL, RO, SE, SK, TH |
| Quantity | 386 units |
| UPC / GTIN / UDI-DI | 00884838004139 |
| Serial numbers | 24079, 24115, 34001, 34011, 34020, 34022, 34023, 34028, 34029, 34030, 34033, 34034, 34038, 34043, 34047, 34052, 34056, 34065, 34066, 34071, 34073, 34074, 34077, 34082, 34085 and 360 more |
| Model numbers | 781177, 781277, 781278, 781344, 781345 |
Product
Achieva 3.0T Model Number (REF): (1) 781345; (2) 781344; (3) 781278; (4) 781277; (5) 781177
Reason for recall
The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
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-1839-2024. 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.