CareFusion 303, Inc. recalls Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092

Recall date

February 12, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1239-2016

FDA classification

Class II

Brand / firm

CareFusion 303, Inc.

Sold / distributed

Nationwide in US: AR, AZ, CA, FL, GA, IN, KY, MD, MI, MN, MO, NJ, NM, NY, OH, OR, PA, SC, TN, TX, VA, WI.

Why it was recalled

CareFusion is recalling the Alaris PC unit because a component on the PC unit power supply may cause a "System Error" or "Missing Battery" error code (120.4630).

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, Infusion Pump Model 8000, Part No. TC10005092