Recall Z-0250-2013— Sunquest Information Systems, Inc.
Class II · Terminated
Class II FDA medical device recall by Sunquest Information Systems, Inc., initiated 2011-11-03, terminated 2012-11-06. FDA's recall record names no specific 510(k) clearance for this event. Product: Sunquest Laboratory, version 7.0 not available. Reason: Sunquest is recalling Sunquest Laboratory version 7.0 because when saving an Accession to a non-current Episode/Event, a User-Defined field can be incorrectly replaced by the current Episode/Event User-Defined data..
- Recalling firm
- Sunquest Information Systems, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2011-11-03
- Terminated
- 2012-11-06
- Firm location
- Tucson, AZ, United States
Product description
Sunquest Laboratory, version 7.0 not available
Reason for recall
Sunquest is recalling Sunquest Laboratory version 7.0 because when saving an Accession to a non-current Episode/Event, a User-Defined field can be incorrectly replaced by the current Episode/Event User-Defined data.
Data sourced from openFDA. This site is unofficial and independent of the FDA.