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FDAFDA · Food and drugs·Recall number Z-2229-2012

Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Product Usage: for clinical use

Published August 29, 2012 · Recall initiated: August 12, 2011

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Sunquest Information Systems, Inc.
Distributor
US Nationwide Distribution
Lot
Version 6.4.2
Risk classification
Class III
Area (FDA)
device
Country
United States

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