FDADecember 21, 2018device

DigitalDiagnost C50, Stationary X-ray System

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

philips healthcarephilips

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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