Misys Healthcare Systems Misys Commercial Laboratory, Laboratory Information System, version 3.4.1 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Misys Commercial Laboratory, Laboratory Information System, version 3.4.1
Brand
Misys Healthcare Systems
Lot Codes / Batch Numbers
Version 3.4.1
Products Sold
Version 3.4.1
Misys Healthcare Systems is recalling Misys Commercial Laboratory, Laboratory Information System, version 3.4.1 due to Software logic error.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software logic error.
Recommended Action
Per FDA guidance
The firm wrote and installed code to correct the problem on 3/13/2003. Recall is complete.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN, SC
Page updated: Jan 10, 2026