FDAAugust 6, 2021device

Affiniti Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: Affiniti 30 795121 Affiniti 30 795218 Affiniti 50 795208 Affiniti 50 795118 Affiniti 70 795210 Affiniti 70 795119

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

The hazard

Due to a software defect that can intermittently cause the system to lock-up which exiting Review Mode while performing an exam.

What to do

FDA enforcement status: Completed

Brands named

philips ultrasoundphilips

UPCs

0088483807418700884838097957

Recall history

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

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Affiniti Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: Affiniti 30 795121 Affiniti 30 795218 Affiniti 50 795208 Affiniti 50 795118 Affiniti 70 795210 Affiniti 70 795119 — Recall Details · AllClear