FDAOctober 9, 2023device

Philips Affiniti 70, Diagnostic Ultrasound System Model # 795210

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

The hazard

Their is the potential that diagnostic ultrasound systems operating with software version 10.0 may present a delayed image instead of a real time image.

What to do

FDA enforcement status: Completed

Brands named

philips ultrasoundphilips

UPCs

00884838106611

Recall history

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

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