Z-0686-03

Misys Laboratory version 5.3

Name: Z-0686-03 Misys Laboratory version 5.3
Creator: Misys Healthcare Systems
Published: 2003-02-28
License: https://open.fda.gov/license/

CliniSys, Inc / initiated 2003-02-28 / Terminated

FDA source

Misys Healthcare Systems began a recall of Misys Laboratory version 5.3 on 2003-02-28. The reason FDA records is "Patient results do not update properly when modified using on-line entry function". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0686-03
Status: Terminated
Initiated: 2003-02-28
Posted: 2003-04-02
Terminated: 2004-06-02
Recalling firm: CliniSys, Inc
Product: Misys Laboratory version 5.3
Product code: JQP Calculator/Data Processing Module, For Clinical Use
Reason for recall: Patient results do not update properly when modified using on-line entry function.
FDA root cause: Other
Action: Product Safety Notice (PSN-03-L10) was sent to all affected clients by fax on 2/28/2003. It contained a procedural workaround. An announcement of the availability of a software upgrade or fix will be made when it is available.
Quantity in commerce: 460
Distribution: Nationwide and to United Kingdom, Ireland, Denmark, Canada, Bermuda, Saudi Arabia, United Arab Emirates.
Product codes and lots: Version 5.3 only.

Product code JQP

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)