Recall Z-2229-2012— Sunquest Information Systems, Inc.
Class III · Terminated
Class III FDA medical device recall by Sunquest Information Systems, Inc., initiated 2011-08-12, terminated 2012-09-04. FDA's recall record names no specific 510(k) clearance for this event. Product: Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Product Usage: for clinical use. Reason: In GUI inquiry, searching by ID (CID) may return the wrong patient demographic data if the accession number associated to the CID is no longer inactive..
- Recalling firm
- Sunquest Information Systems, Inc.
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2011-08-12
- Terminated
- 2012-09-04
- Firm location
- Tucson, AZ, United States
Product description
Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Product Usage: for clinical use
Reason for recall
In GUI inquiry, searching by ID (CID) may return the wrong patient demographic data if the accession number associated to the CID is no longer inactive.
Data sourced from openFDA. This site is unofficial and independent of the FDA.