Reported Oct 2, 2019 · Terminated

DigitalDiagnost C50, Stationary X-ray System

Philips Healthcare

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips Healthcare · 3000 Minuteman Rd · Andover, MA · 01810-1032

Is this the product you have?

  • DigitalDiagnost C50, Stationary X-ray System
Lot codes and dates
  • Product
  • Number 712201 System Serial NumberSN170053 SN180074
Amount recalled
2

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 27, 2020 · Data as of Sep 19, 5:35 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.