FDAFebruary 6, 2013device

Plum A+3 Infusion Pump. List Number 12391. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor based infusion devi...

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

The hazard

The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.

What to do

FDA enforcement status: Terminated

Brands named

hospira

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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