ICU recalls The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies…

Recall date

February 1, 2013

Source

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

Recall number

Z-2678-2017

FDA classification

Class II

Brand / firm

ICU

Sold / distributed

Nationwide, Worldwide

Why it was recalled

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

The Plum A+ Infusion Systems are a multipurpose 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 devices. The pumps are available in single channel and in triple channel pumping mechanism types.