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

Recall Z-0598-2017 — IQon Spectral CT Computed Tomography X-ray system, Model 728332

U.S. FDA — Device Enforcement · United States · 2016-10-13 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0598-2017
Date of alert
2016-10-13
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Philips Medical Systems (Cleveland) Inc
Product category
device
Product type
Devices
Reported risk: The product label does not include the correct current rating.
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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