# FDA recall Z-2256-2020

> **Philips North  America, LLC** · Class II · device recall initiated 2020-04-23.

## Product

ProxiDiagnost N90, UDI 706100

## Reason for recall

The thermo switches in the three-phase transformer, which normally aid in powering down the System Power Distribution Unit, may be incorrectly installed and not working. If the transformer overheats due to a first failure and the thermo switch is not activated, the device may begin to generate smoke.

## Distribution

Domestic distribution nationwide. Foreign distribution to Chile and Germany.

## Key facts

- **Recall number:** Z-2256-2020
- **Recalling firm:** Philips North  America, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-23
- **Report date:** 2020-06-10
- **Termination date:** 2023-03-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Andover, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2256-2020

## Citation

> AI Analytics. FDA recall Z-2256-2020. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-2256-2020. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*