Misys Healthcare Systems Misys Laboratory System versions 5.23 and 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 versions 5.23 and 5.3
Brand
Misys Healthcare Systems
Lot Codes / Batch Numbers
Versions 5.23 and 5.3
Products Sold
Versions 5.23 and 5.3
Misys Healthcare Systems is recalling Misys Laboratory System versions 5.23 and 5.3 due to With SMART enabled, for an accession number with multiple tests, credits and additions, the system may delete and reorder resulted tests.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
With SMART enabled, for an accession number with multiple tests, credits and additions, the system may delete and reorder resulted tests.
Recommended Action
Per FDA guidance
The firm faxed notification on 3/26/2003 along with a response form and a temporary procedural workaround in Product Safety Notice PSN-03-L13.
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