# FDA recall Z-2154-2017

> **Philips Electronics North  America Corporation** · Class II · device recall initiated 2017-05-11.

## Product

Philips DigitalDiagnost 3.1.x X-Ray System

## Reason for recall

During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have identified a potential issue that may affect the performance of the equipment under certain conditions.

## Distribution

USA(nationwide) Distribution to the states of : AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KY, LA, MA, ME, MI, MN, MO, NC, ND, NE, NH, NM, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA and WI

## Key facts

- **Recall number:** Z-2154-2017
- **Recalling firm:** Philips Electronics North  America Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-11
- **Report date:** 2017-06-21
- **Termination date:** 2018-07-10

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2154-2017

## Citation

> AI Analytics. FDA recall Z-2154-2017. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-2154-2017. Source: US FDA. Licensed CC0.

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