Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-3217-2024 — ACUSON Maple 1.0 Diagnostic Ultrasound System, REF: 11711750, with software. ACUSON Maple Select 1.0 Diagnostic Ultrasound System, REF: 11711779, with software

U.S. FDA — Device Enforcement · United States · 2024-08-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3217-2024
Date of alert
2024-08-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
11711750
Reported risk: 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
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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