Misys Healthcare Systems Misys Laboratory System, versions 5.3 build 63 through 5.3.2 and LabAccess Results. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Misys Laboratory System, versions 5.3 build 63 through 5.3.2 and LabAccess Results.
Brand
Misys Healthcare Systems
Lot Codes / Batch Numbers
Version 5.3 build 63 thru 6.3.2 and LabAccess Results.
Products Sold
Version 5.3 build 63 thru 6.3.2 and LabAccess Results.
Misys Healthcare Systems is recalling Misys Laboratory System, versions 5.3 build 63 through 5.3.2 and LabAccess Results. due to Incorrect demographics display which can result in incorrect information being used in diagnosis or treatment of patients.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect demographics display which can result in incorrect information being used in diagnosis or treatment of patients.
Recommended Action
Per FDA guidance
A temporary procedural workaround was communicated by fax to customers in Product Safety Notice PSN-03-L33 on July 21, 2003. Asecond Notice (L33A) was sent to customers to futher facilitate the recall.
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