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

Recall Z-1695-2016 — Philips Healthcare DigitalDiagnost stationary X-ray system

U.S. FDA — Device Enforcement · United States · 2015-11-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1695-2016
Date of alert
2015-11-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips Healthcare
Product category
device
Product type
Devices
Reported risk: The detector may signal that it is ready for acquisition when it actually is not, resulting in failure to properly acquire the X-ray image.
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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