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Becton Dickinson & Company recalls BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a h
Recalled March 16, 2016 · FDA recall Z-1076-2016 · Becton Dickinson &
Hazard
The sterility of the product cannot be assured. This may result in increased risk of infection. · FDA Class II
Units
250 units
Sold at
US Distribution to:California and Utah.
Description
The sterility of the product cannot be assured. This may result in increased risk of infection.
Product
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.
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →