CareFusion 303, Inc. recalls Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
- Recall date
- February 15, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1179-2016
- FDA classification
- Class II
- Brand / firm
- CareFusion 303, Inc.
- Sold / distributed
- Michigan
Why it was recalled
CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set.
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 Pump VersaSafe Infusion Set, Model No. 2122-0007
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