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

Alere Triage¿ TOX Drug Screen Control 1 Product Generic Name: Quality Control Material Description of the product: Good Laboratory Practice suggests that external controls should be tested with each new lot or shipment of test materials, or every 30 days, and as otherwise required by a labor — recall Z-0053-2014

U.S. FDA — Device Enforcement · United States · 2013-09-23 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0053-2014
Date of alert
2013-09-23
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Alere San Diego, Inc.
Product category
device
Product type
Devices
Reported risk: Alere San Diego, Inc. initiated a voluntary recall of Alere Triage TOX Drug Screen Control 1 (PN 94413, Lot C2681A) because the CODE CHIP that was provided with this lot causes the control to fail when run in the QC Sample Mode using Alere Triage TOX Drug Screeen products. The Alere Triage TOX Drug Screen test devices and patient results are not affected.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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