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

Recall Z-0035-2014 — IMPAX 5.2 DB Server (running Oracle 10.1.0.4.0), medical imaging Picture Archiving and Communication System (PACS).

U.S. FDA — Device Enforcement · United States · 2013-09-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0035-2014
Date of alert
2013-09-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
AGFA Corp.
Product category
device
Product type
Devices
Reported risk: System downtime and/or slow performance may result if software in use is an old version of IMPAX and is not at current supported levels.
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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