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

Recall Z-1249-2024 — MRI system: Vantage Elan, Model: MRT-2020

U.S. FDA — Device Enforcement · United States · 2024-01-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1249-2024
Date of alert
2024-01-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Canon Medical System, USA, INC.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04987670101632
Reported risk: For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in "System Information" of the operation window and some of the maximum SFG values described in the safety manual are lower than the correct values, which may cause a patient with an MR conditional device to feel some discomfort during the MR scan.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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