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

Recall Z-2314-2012 — TxRx Knee 15 Coil 3T. For use in conjunction with magnetic resonance scanners to produce diagnostic images of the knee that can be interpreted by a trained physician.

U.S. FDA — Device Enforcement · United States · 2012-07-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2314-2012
Date of alert
2012-07-27
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Quality Electrodynamics LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10606829
Reported risk: On July 27, 2012, it was reported to the firm that the Siemens 3T 15ch Knee Coil was not functional because the coil identification code for the device was incorrect.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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