# FDA recall Z-2498-2019

> **Philips Healthcare** · Class II · device recall initiated 2018-12-21.

## Product

DigitalDiagnost C50, Stationary X-ray System

## Reason for recall

During recent evaluations of the Philips DigitalDiagnost C50 system, Philips identified a missing label.  This notification is intended to provide you with information regarding what the issue is, and relevant affected product, the actions you are required to take and the actions planned by Philips to correct the issue.  If you need any or further information or support concerning this issue, please contact your local Philips representative or Philips Customer Service: 1-800-722-9377.

## Distribution

Puerto Rico

## Key facts

- **Recall number:** Z-2498-2019
- **Recalling firm:** Philips Healthcare
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-12-21
- **Report date:** 2019-10-02
- **Termination date:** 2020-10-27

- **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-2498-2019

## Citation

> AI Analytics. FDA recall Z-2498-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2498-2019. Source: US FDA. Licensed CC0.

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