Misys Healthcare Systems Misys Laboratory System version 5.3 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Misys 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 Misys Laboratory System version 5.3 due to Patient files become mixed up due to a software defect.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Patient files become mixed up due to a software defect.
Recommended Action
Per FDA guidance
Client was faxed a notice. All duplicate order numbers were identified, corrected and resent to the hospital system.
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
NY
Page updated: Jan 10, 2026