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

Recall Z-2272-2012 — Sunquest Laboratory LabAccess Results Workstation (LARS)

U.S. FDA — Device Enforcement · United States · 2010-10-05 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2272-2012
Date of alert
2010-10-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Sunquest Information Systems, Inc.
Product category
device
Product type
Devices
Reported risk: 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.
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.

Related

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.