FDAJune 30, 2020device

Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may lead to interruption of communication or power between PC Unit and modules, which may result in an infusion that stops with a CHANNEL DISCONNECTED message, and an audio/visual alarm on the PC Unit and an interruption of therapy or monitoring.

What to do

FDA enforcement status: Terminated

Brands named

carefusion 303carefusion

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →
Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system — Recall Details · AllClear