Philips Healthcare: Medical Device Recall in 2019 - (Recall #: Z-2498-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

DigitalDiagnost C50, Stationary X-ray System

Product Classification:

Class II

Date Initiated: December 21, 2018

Date Posted: October 2, 2019

Recall Number: Z-2498-2019

Event ID: 83654

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.

Status: Terminated

Product Quantity: 2

Code Information:

Product Number 712201 System Serial Number: SN170053 SN180074

Distribution Pattern:

Puerto Rico

Voluntary or Mandated:

FDA Mandated