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

Recall Z-2059-2013 — Philips Easy Upgrade DR, Code No: 712086 This system is used for making X-Ray exposures for diagnostics.

U.S. FDA — Device Enforcement · United States · 2013-08-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2059-2013
Date of alert
2013-08-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips Healthcare Inc.
Product category
device
Product type
Devices
Reported risk: The mirror icon on the bottom of each image could be misinterpreted as a RIGHT lead marker for side indication if the image is mirrored within a PACS system.
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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