Misys Healthcare Systems Misys Commercial Laboratory version 2.x thru 3.4.1 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 Commercial Laboratory version 2.x thru 3.4.1
Brand
Misys Healthcare Systems
Lot Codes / Batch Numbers
Versions 2.x through 3.4.1
Products Sold
Versions 2.x through 3.4.1
Misys Healthcare Systems is recalling Misys Commercial Laboratory version 2.x thru 3.4.1 due to Urgent care STAT reports are not printing in a timely fashion.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Urgent care STAT reports are not printing in a timely fashion.
Recommended Action
Per FDA guidance
Recall notifications were sent to users on April 1, 2003 in Product Safety Notice PSN-03-L16 by facsimile.
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