RecallRadar

FDA Device recall Z-3217-2024

ACUSON Maple 1.0 Diagnostic Ultrasound System, REF: 11711750, with software

On 2024-10-02 the FDA classified a Class II recall of ACUSON Maple 1.0 Diagnostic Ultrasound System, REF: 11711750, with software by Siemens Medical Solutions Usa, citing if ultrasound systems with software, are changed from factory default to : 1) Milliliters per second (ml/sec, mL/sec) or 2) Milliliters per minute (ml/min, mL/min); then systems w….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-3217-2024
ClassificationClass II
Statusongoing
Initiated2024-08-15
Published2024-10-02
Last updated2026-09-13 11:57 UTC
CompanySiemens Medical Solutions Usa
DistributionAL, AR, AZ, CA, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NY, OH, OK, OR, PR, RI, SC, SD, TN, TX, VA, WA, WI, WY

Product

ACUSON Maple 1.0 Diagnostic Ultrasound System, REF: 11711750, with software. ACUSON Maple Select 1.0 Diagnostic Ultrasound System, REF: 11711779, with software

Reason

If ultrasound systems with software, are changed from factory default to : 1) Milliliters per second (ml/sec, mL/sec) or 2) Milliliters per minute (ml/min, mL/min); then systems will perform incorrect unit conversion of liters to milliliters using multiplier 100 instead of 1000, resulting values 10x smaller than actual, which could contribute misdiagnosis or negatively influence patient management

Identifiers

code_info11711750, UDI-DI: 04056869995809, Software VA10A 11711779, UDI-DI: 04056869995830, Software VA10A

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3217-2024%22

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