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

Recall Z-0439-2021 — Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and RTLR180343

U.S. FDA — Device Enforcement · United States · 2020-09-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0439-2021
Date of alert
2020-09-12
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: The device may detect an incorrect Heater Bag volume which may lead to a 'Supply Bag Line Blocked' alarm during treatment. This alarm may cause the Heater Bag to contain more fluid than expected and the cycler does not recognize the extra fluid is present and it will not make it available for treatment. Not having enough solution to complete treatment may lead to inadequate dialysis which could result in the accumulation of toxins and fluid. Symptoms may include shortness of breath, increased weight gain, and increased blood pressure.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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