# FDA recall Z-2523-2020

> **Philips North  America, LLC** · Class II · device recall initiated 2020-06-02.

## Product

EasyDiagnost Eleva DRF, model no. 706050 - Product Usage: X-ray system, diagnostic, general-purpose.

## Reason for recall

Thermo switches in the main power supply for the system may be incorrectly installed, resulting in a malfunction.

## Distribution

Worldwide distribution - US Nationwide distribution including in the states of AR, AZ, CA, CT, FL, GA, HI, IL, LA, MA, MD, MI, MS, MT, NC, NY, TN, TX and the country of Panama.

## Key facts

- **Recall number:** Z-2523-2020
- **Recalling firm:** Philips North  America, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-02
- **Report date:** 2020-07-15
- **Termination date:** 2021-02-09

- **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-2523-2020

## Citation

> AI Analytics. FDA recall Z-2523-2020. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-2523-2020. Source: US FDA. Licensed CC0.

---

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