Becton Dickinson & Company recalls BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a hos…

Recall date

December 9, 2015

Source

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

Recall number

Z-1076-2016

FDA classification

Class II

Brand / firm

Becton Dickinson & Company

Sold / distributed

US Distribution to:California and Utah.

Why it was recalled

The sterility of the product cannot be assured. This may result in increased risk of infection.

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

What was recalled

BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a hospital or medical center setting with patients who are receiving manually administered bolus intravenous injections as part of their care to facilitate documentation of the medications.