Atlas FDA

Misys Laboratory, GUI version 5.3

FDA device recall Z-0495-03 · posted 2003-01-30 · Terminated

Recall details

Recalling firm
Misys Healthcare Systems
Reason for recall
An incorrect collection date and time may be accepted and filed to the patient file.
Action taken
The firm's recall notice was sent by fax to all customers on Jan. 3, 2003. It communicated a procedural workaround and the availability of product corrections.
Root cause
Other
Status
Terminated
Product code
JQP
Quantity affected
465
Distribution
Nationwide and to United Kingdom, Ireland, Canada, Denmark, Bermuda, Saudi Arabia, United Arab Emirates.
Date initiated
2002-12-20
Date posted
2003-01-30
Date terminated
2004-12-01
Location
Tucson, AZ

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.