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

Recall Z-1750-2019 — Discovery Ml DR Product Usage: The systems are intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging and localization of emission activity in patient anatomy by means of integrated PET and CT images.

U.S. FDA — Device Enforcement · United States · 2019-02-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1750-2019
Date of alert
2019-02-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Healthcare, LLC
Product category
device
Product type
Devices
Reported risk: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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