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Hitachi Medical Systems America Inc recalls Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic Ult
Recalled May 24, 2017 · FDA recall Z-2090-2017 · Hitachi Medical Systems America
Hazard
The strength of the arm mounting mechanism was insufficient and had to be redesigned. · FDA Class II
Units
77
Sold at
Distributed to the states of: AZ, CA, FL, HI, IL MA, MD, ME, MN, MO, NC, NJ, NY, OH, PA, SC, TN, and TX.
Description
The strength of the arm mounting mechanism was insufficient and had to be redesigned.
Product
Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic Ultrasound evaluation.
Manufacturer(s)
Hitachi Medical Systems America Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →