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

Recall Z-2315-2012 — Toshiba Ultra-Short Magnetic Resonance Imaging System, EXCELART Vantage. MRT-1503/P5-Vantage MRI System. MR imaging.

U.S. FDA — Device Enforcement · United States · 2012-02-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2315-2012
Date of alert
2012-02-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Toshiba American Medical Systems Inc
Product category
device
Product type
Devices
Reported risk: The firm recalled due to a potentail problem with the position of the hold in the lug teminals on the power cables connected to the terminal blocks on the gradient coil.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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