FDAMay 2, 2017device

Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic Ultrasound evaluation.

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

The hazard

The strength of the arm mounting mechanism was insufficient and had to be redesigned.

What to do

FDA enforcement status: Terminated

Brands named

hitachi medical systems americahitachihitachi medical

Recall history

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

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