FDAApril 29, 2019device

Philips EPIQ and Affiniti Ultrasound Systems with software version 4.0: Models EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIZ CVx, Affiniti 30, Affiniti 50, and Affiniti 70. Product Usage: The intended use of the EPIQ, EPIQ 5, EPIQ 7, Affiniti 30, Affiniti 50 and Affiniti 70 Diagnosti...

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

The hazard

There is a potential that the image of one patient could get unexpectedly moved into another patient's folder when the user is using the Edit functionality on the Patient Data Entry (PDE) screen of the device.

What to do

FDA enforcement status: Terminated

Brands named

philips ultrasoundphilips

Recall history

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

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