FDAFebruary 15, 2016device

Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007

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

The hazard

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.

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.

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Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007 — Recall Details · AllClear