Misys Healthcare Systems Misys Laboratory System versions 5.2, 5.23, 5.3, 5.3.1 and 5.3.2. 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 5.2, 5.23, 5.3, 5.3.1 and 5.3.2.
Brand
Misys Healthcare Systems
Lot Codes / Batch Numbers
versions 5.2, 5.23, 5.3, 5.3.1 and 5.3.2.
Products Sold
versions 5.2, 5.23, 5.3, 5.3.1 and 5.3.2.
Misys Healthcare Systems is recalling Misys Laboratory System versions 5.2, 5.23, 5.3, 5.3.1 and 5.3.2. due to Incorrect results could be filed.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect results could be filed.
Recommended Action
Per FDA guidance
The firm sent Product Safety Notice PSN-03-L18 by fax to customers on 4/14/2003.
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