Philips Digital Diagnost radiographic system Cl ll

Company:Philips Healthcare Inc
Date of Enforcement Report 3/13/2013
Class ll:

PRODUCT

Philips Digital Diagnost Stationary radiographic system. Recall Number Z-0900-2013

REASON
When the operator for a wall stand view selects an “image rotation” different from default, or such image rotation is preset in the examination database, then the resulting image may be rotated in the wrong direction. When the operator manually rotates the image back, electronic side markers (if programmed) are rotated also and as a result may be placed in a wrong position inside the image.

RECALLING FIRM/MANUFACTURER
Philips Healthcare Inc, Andover, MA on 10/30/2012. Voluntary: Firm Initiated recall is ongoing.

VOLUME OF PRODUCT IN COMMERCE
360

DISTRIBUTION
Nationwide and Internationally

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About the author

Amy enjoys researching and writing about developments in medical technology and how that intersects with US law. She received her J.D. from the University of Florida Levin College of Law in 2020 and now works as a Regulatory Associate for SoftwareCPR®, a general-purpose regulatory consulting firm that is recognized globally for their expertise with standards and national regulations pertaining to medical device, mobile medical app, and HealthIT software.

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