Medical device recalls Moderate risk

CareFusion 303, Inc. recalls Alaris PC unit, Model 8015 The Alaris PC unit is the central programming, monitoring and power supply component for the…

Recall date
March 24, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1606-2016
FDA classification
Class II
Brand / firm
CareFusion 303, Inc.
Sold / distributed
Worldwide Distribution: US (nationwide) and countries of: Australia, Great Britain and Canada.

Why it was recalled

The Alaris PC units model 8015 may display a system error code 133.6080 due to failure with the super capacitor (C245) at power up on the Alaris PC unit logic boards.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Alaris PC unit, Model 8015 The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System.

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