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

Recall Z-1618-2014 — Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards and also sold as replacement parts for use with Fresenius 2008-Series Hemodialysis Machines (2008K, 2008K2, 2008K@home and 2008T). Part Number: 190234 Revision K

U.S. FDA — Device Enforcement · United States · 2014-04-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1618-2014
Date of alert
2014-04-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Fresenius Medical Care Holdings, Inc.
Product category
device
Product type
Devices
Reported risk: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may fail to detect a disconnected Ultrafiltration (UF) Pump
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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