Misys Healthcare Systems Misys Laboratory System, Versions 5.2, 5.23, 5.3 up to 5.3.2. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Misys Laboratory System, Versions 5.2, 5.23, 5.3 up to 5.3.2.
Brand
Misys Healthcare Systems
Lot Codes / Batch Numbers
Versions 5.2, 5.23, 5.3 up to 5.3.2.
Products Sold
Versions 5.2, 5.23, 5.3 up to 5.3.2.
Misys Healthcare Systems is recalling Misys Laboratory System, Versions 5.2, 5.23, 5.3 up to 5.3.2. due to Software defect causes orders to be lost under certain conditions of use. A typographical error at the Accept/Modfy/Reject prompt will cause the orde. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software defect causes orders to be lost under certain conditions of use. A typographical error at the Accept/Modfy/Reject prompt will cause the order not to be processed by the system.
Recommended Action
Per FDA guidance
Product Safety Notice PSN-03-L32 was issued by fax to customers on July 7, 2003. It communcated a procedural workaround and that a follow-up notification was pending completion of a software engineering project to correct the defect.
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