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

Recall Z-2468-2024 — Optima MR450w 1.5T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0, DV29.1, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System

U.S. FDA — Device Enforcement · United States · 2024-06-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2468-2024
Date of alert
2024-06-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Medical Systems, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
1000004458
Reported risk: GE HealthCare has become aware that for certain MR systems, the system predicted B1+RMS value can exceed the B1+RMS user prescribed limit when scanning in Low SAR Mode and the following two conditions are met: 1. 2D FSE T2 FLAIR OR T2 FLAIR Propeller imaging sequence is selected, AND 2. the Optimized T2 FLAIR sequence option is turned off OR not included in the MR configuration. If this occurs, it can result in overheating of an MR conditional implant.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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