Ingenia Ambition S — Class II medical device recall Z-1240-2019
Terminated recall by Philips Medical Systems Nederlands, reported 2019-05-08, distributed in FL. Magnet Energization Device (MED) can have a residual voltage on output terminal, may cause electrical shocks t
| Recall number | Z-1240-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems Nederlands, Best, N/A, Netherlands |
| Recall initiated | 2019-03-25 |
| Classified | 2019-04-26 |
| Reported by FDA | 2019-05-08 |
| Terminated | 2020-06-04 |
| Distributed | FL |
| Countries outside the US | CH, DE |
| Quantity | 4 units |
| Serial numbers | 47001, 47002, 47004OUS, 48000 |
Product
Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED), Philips MR systems are indicated for use as a diagnostic device. The purpose of the MED is to supply power to charge the magnet. MED is abbreviation for Magnet Energize Device
Reason for recall
Magnet Energization Device (MED) can have a residual voltage on output terminal, may cause electrical shocks to personnel servicing the MED, MDD or connected cabling.
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-1240-2019. 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.