Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) Recalled by Siemens Medical Solutions USA, Inc. Due to Software issues with ACUSON SC2000 ultrasound with software...
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 Siemens Medical Solutions USA, Inc. directly.
Affected Products
ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35); ultrasound imaging system.
Quantity: 257 units
Why Was This Recalled?
Software issues with ACUSON SC2000 ultrasound with software version 3/5 (VA35) - may incorrectly display the color flow data in the wrong position and when Doppler Frequency is adjusted, the system does not restart the pulsed wave Doppler or continuous wave Doppler waveform.
Where Was This Sold?
This product was distributed to 30 states: AL, AZ, AR, CA, CO, CT, FL, GA, ID, IL, IN, KS, MD, MI, MN, MO, NH, NY, NC, OH, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI
About Siemens Medical Solutions USA, Inc.
Siemens Medical Solutions USA, Inc. has 87 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report