Misys Healthcare Systems Misys Laboratory System version 5.3 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 Laboratory System version 5.3
Brand
Misys Healthcare Systems
Lot Codes / Batch Numbers
Version 5.3 only.
Products Sold
Version 5.3 only.
Misys Healthcare Systems is recalling Misys Laboratory System version 5.3 due to Software anomally, One client reported patient tests and results are deleted when duplicate orders are placed.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software anomally, One client reported patient tests and results are deleted when duplicate orders are placed.
Recommended Action
Per FDA guidance
Notice was sent by fax on 4/1/2003 under Product Safety Notice, PSN-03-L17. A code modification is yet to be released. Customers have been provided with a temporary workaround procedure.
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
MI, NY, OH
Page updated: Jan 10, 2026