Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Diagnostics Ultrasound System Ultrasounds System Sonimage HS1 Recalled by Konica Minolta, Inc. Due to The Doppler velocity measurement on the Sonimage HS1...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Konica Minolta, Inc. directly.
Affected Products
Diagnostics Ultrasound System Ultrasounds System Sonimage HS1
Quantity: 36 units
Why Was This Recalled?
The Doppler velocity measurement on the Sonimage HS1 ultrasound system is not accurate.
Where Was This Sold?
This product was distributed to 9 states: CA, CO, FL, IA, KY, NJ, NY, TX, WA
About Konica Minolta, Inc.
Konica Minolta, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report