Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2229-2012 — Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Product Usage: for clinical use

U.S. FDA — Device Enforcement · United States · 2011-08-12 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2229-2012
Date of alert
2011-08-12
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Sunquest Information Systems, Inc.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.