Misys Healthcare Systems Mysys Laboratory System Version 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
Mysys Laboratory System Version 5.3
Brand
Misys Healthcare Systems
Lot Codes / Batch Numbers
Version 5.3.
Products Sold
Version 5.3.
Misys Healthcare Systems is recalling Mysys Laboratory System Version 5.3 due to Abnormal results are flagged as normal.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Abnormal results are flagged as normal.
Recommended Action
Per FDA guidance
This is a completed recall. Consignee has had the software patch installed and reports it to be functional as of March 19, 2003. Recall notice was also sent that same day.
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 noticeDistribution
As reported by FDA
IN, NE
Page updated: Jan 10, 2026