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

Recall Z-2751-2018 — Monitor with one Blood Parameter Module and one HSat Probe; 500AHCT Monitor with two Blood Parameter modules and one HSat Probe; 500AVHCT Product Usage: The CDI System 500 provides continuous, on-line monitoring of the extracorporeal partial pressure of oxygen and carbon dioxide, pH, potassium,

U.S. FDA — Device Enforcement · United States · 2018-06-26 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2751-2018
Date of alert
2018-06-26
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Terumo Cardiovascular Systems Corporation
Product category
device
Product type
Devices
Reported risk: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat population, which has resulted in an increase of Hybrids failing the H/Sat Color Chip Test which is an automated self-test when the device is powered on. This will not result in device inaccuracy, only Color Chip Test Failure which disables the H/Sat module.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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