Konica Minolta, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2769-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Diagnostics Ultrasound System Ultrasounds System Sonimage HS1

Product Classification:

Class II

Date Initiated: April 24, 2017

Date Posted: August 2, 2017

Recall Number: Z-2769-2017

Event ID: 77712

Reason for Recall:

The Doppler velocity measurement on the Sonimage HS1 ultrasound system is not accurate.

Status: Terminated

Product Quantity: 36 units

Code Information:

UDI 04560141940031 04560141944534 04560141945463 04560141946385 V1.31R02 V1.31R04 V1.31R05 V1.31R06 (V131R02 SW and later version)

Distribution Pattern:

CA, CO, KY, FL, NJ, NY, IA TX, & WA

Voluntary or Mandated:

Voluntary: Firm initiated