Misys Healthcare Systems Misys Laboratory 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 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 version 5.3 due to Patient results do not update properly when modified using on-line entry function.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Patient results do not update properly when modified using on-line entry function.
Recommended Action
Per FDA guidance
Product Safety Notice (PSN-03-L10) was sent to all affected clients by fax on 2/28/2003. It contained a procedural workaround. An announcement of the availability of a software upgrade or fix will be made when it is available.
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 noticePage updated: Jan 10, 2026