Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

Reference Library Interface Version 5.3

FDA Recall Z-0497-03 · Posted 2003-01-30

Recalling FirmSunquest Information Systems
Recall StatusTerminated
Product CodeJQP
Date Initiated2002-12-06
Date Terminated2013-02-26
Product Quantity30

Reason for Recall

Software system defect resulting in incomplete patient results information.

Firm Action

Product Safety Notice, PSN-02-L31 will be faxed to all affected customers. The notice provides product users with a description of the problem, an effective workaround, and the estimated release of coding modifications to the software version impacted.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑