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

Recall Z-0190-2022 — Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3

U.S. FDA — Device Enforcement · United States · 2021-10-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0190-2022
Date of alert
2021-10-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
FujiFilm Healthcare Americas Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04562122958974
Reported risk: Diagnostic ultrasound system with the specified software version and used in conjunction with a Fujifilm (formally Hitachi) transducer does not display the measurement results correctly with two cardiology measurement functions: Mitral Regurgitation Flow (MR Flow) Measurement; Mitral Valve (MV) Measurement. In addition there is an error in the instruction manual.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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