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

Recall Z-0703-2019 — Discover VH/Millennium VG Nuclear Medicine Imaging System

U.S. FDA — Device Enforcement · United States · 2017-10-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0703-2019
Date of alert
2017-10-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Healthcare, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
36478041
Reported risk: A potential hazardous situation may occur if the collimator locking handle is not properly placed in the lock position and the warning circuit does not detect that the collimator is unlocked because of the patient proximity to the collimator during a clinical scan.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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