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

ACL TOP 700 LAS, automated coagulation laboratory instrument. — recall Z-2063-2014

U.S. FDA — Device Enforcement · United States · 2014-06-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2063-2014
Date of alert
2014-06-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Instrumentation Laboratory Co.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
08120100
Reported risk: Potential for sample misidentification.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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