# FDA recall Z-1240-2019

> **Philips Medical Systems Nederlands** · Class II · device recall initiated 2019-03-25.

## 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.

## Distribution

US Distribution to state of: FL and Internationally to: Switzerland and Germany.

## Key facts

- **Recall number:** Z-1240-2019
- **Recalling firm:** Philips Medical Systems Nederlands
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-25
- **Report date:** 2019-05-08
- **Termination date:** 2020-06-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Best, N/A, Netherlands

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1240-2019

## Citation

> AI Analytics. FDA recall Z-1240-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1240-2019. Source: US FDA. Licensed CC0.

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