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

Misys Laboratory versions 5.2, 5.23, or 5.3 with ADT Interface to CoPathPlus.

FDA Recall Z-0325-03 · Posted 2002-12-11

Recall StatusTerminated
Product CodeJQP
Date Initiated2002-10-24
Date Terminated2013-02-26
Product Quantity190

Reason for Recall

Interfacing software systems have inconsistent character recognition characteristics.

Firm Action

A recall notice was sent to hospitals on October 24, 2002. It communicated a temporary procedure to work around the problem. Also mentioned was the availabllity of a utility to detect and report suspected duplicate Medical Record Numbers.

Root Cause

Other

Distribution Pattern

Nationwide and to Denmark, Bermuda, United Kingdom, Saudi Arabia, Canada.

Official Source

View FDA Recall →

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

↑