Philips Healthcare Mobile Diagnostic X-Ray System with Digital Panel recall — FDA Z-1706-2017
When the operator moves an image to another view then the electronic marker might be placed at the wrong anatomical position in the resulting image.
Overview of recall records associated with Philips Healthcare Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
When the operator moves an image to another view then the electronic marker might be placed at the wrong anatomical position in the resulting image.
This page summarizes recall records in which the official source identifies Philips Healthcare Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.