Recall Z-2272-2012— Sunquest Information Systems, Inc.
Class II · Terminated
Class II FDA medical device recall by Sunquest Information Systems, Inc., initiated 2010-10-05, terminated 2012-08-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Sunquest Laboratory LabAccess Results Workstation (LARS). Reason: The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory LabAccess Results Workstation (LARS) may file results to the wrong patient by incorrectly combining results..
- Recalling firm
- Sunquest Information Systems, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2010-10-05
- Terminated
- 2012-08-24
- Firm location
- Tucson, AZ, United States
Product description
Sunquest Laboratory LabAccess Results Workstation (LARS)
Reason for recall
The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory LabAccess Results Workstation (LARS) may file results to the wrong patient by incorrectly combining results.
Data sourced from openFDA. This site is unofficial and independent of the FDA.