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Konica Minolta, Inc. recalls Diagnostics Ultrasound System Ultrasounds System Sonimage HS1
Recalled August 2, 2017 · FDA recall Z-2769-2017 · Konica Minolta
Hazard
The Doppler velocity measurement on the Sonimage HS1 ultrasound system is not accurate. · FDA Class II
Units
36 units
Sold at
CA, CO, KY, FL, NJ, NY, IA TX, & WA
Description
The Doppler velocity measurement on the Sonimage HS1 ultrasound system is not accurate.
Product
Diagnostics Ultrasound System Ultrasounds System Sonimage HS1
Manufacturer(s)
Konica Minolta, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →