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

Recall Z-1588-2013 — Brilliance CT 64, Ingenuity CT, Ingenuity Core, and Ingenuity Core128 scanners are whole body Computed Tomography X-ray systems. Produce cross-sectional images of the body by computer reconstruction of x-ray transmission.

U.S. FDA — Device Enforcement · United States · 2013-03-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1588-2013
Date of alert
2013-03-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips Medical Systems (Cleveland) Inc
Product category
device
Product type
Devices
Reported risk: If the operator selects a patient name from the worklist using the mouse and then selects a different patient name using the keyboard (arrow keys then press enter) the patient name that populates the exam information page is the patient name selected with the mouse. Also, it is possible to begin a normal clinical scan while the anti-virus scan is running. However, if the user is running a bol
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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