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

Recall Z-1520-2017 — Alaris System PC unit, model no. 8000 and 8015. The central programming, monitoring and power supply component for the Alaris infusion pump System.

U.S. FDA — Device Enforcement · United States · 2016-11-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1520-2017
Date of alert
2016-11-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CareFusion 303, Inc.
Product category
device
Product type
Devices
Reported risk: Reports where the Low Battery alarm and/or the Very Low Battery alarm are not being triggered before the battery is discharged and all infusion channels are stopped.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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