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

Recall Z-1667-2018 — Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version 6) 35700BAXRE Product Usage: The Baxter Sigma Spectrum Infusion Pump with master Drug Library is intended to be used for the controlled administration of fluids. These fluids may includes pharmaceutical drugs, blood, blood pro

U.S. FDA — Device Enforcement · United States · 2018-04-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1667-2018
Date of alert
2018-04-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Reported risk: Service technician improperly documented final release testing on product, indicating that the full battery of release tests were performed when, in fact, several tests were omitted. he omitted tests include air-in-line detection at 400ml/hr and 800ml/hr and verification of upstream occlusion detection at 800ml/hr. Improper detection of air-in-line or upstream occlusion may result in serious adverse health consequences.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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