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

Recall Z-2060-2014 — ACL TOP (Base), automated coagulation laboratory instrument.

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-2060-2014
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)
03110101
Reported risk: Potential for sample misidentification.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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