ClearanceBrief
Recall Z-0807-03 ยท

Misys Healthcare Systems

Misys Laboratory System version 5.3

DateMay 9, 2003 (initiated Apr 1, 2003)
StatusTerminated
ReasonSoftware anomally, One client reported patient tests and results are deleted when duplicate orders are placed.
Root causeOther
ActionNotice was sent by fax on 4/1/2003 under Product Safety Notice, PSN-03-L17. A code modification is yet to be released. Customers have been provided with a temporary workaround procedure.
Quantity3
DistributionStates of MI, OH, NY.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.