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

Recall Z-1345-2013 — TD-Synergy. Laboratory Information System.

U.S. FDA — Device Enforcement · France · 2010-07-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1345-2013
Date of alert
2010-07-29
Country / jurisdiction
France
Risk level
Class II
Risk type
recall
Brand
Technidata S.A.
Product category
device
Product type
Devices
Reported risk: Technidata has discovered that using the F8 key in the ERM session to add a combined test can result in the modification of the value of a result that has already been entered for a test of the request.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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