CareFusion 303, Inc. recalls Alaris PC units, Model No. 8015. Infusion pump.
- Recall date
- March 12, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1311-2015
- FDA classification
- Class II
- Brand / firm
- CareFusion 303, Inc.
- Sold / distributed
- Worldwide Distribution - USA (nationwide), Canada, European Union, Singapore and Australia.
Why it was recalled
CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a keypad issue.
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 units, Model No. 8015. Infusion pump.
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