Becton Dickinson & Company: Medical Device Recall in 2016 - (Recall #: Z-1076-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: December 9, 2015

Date Posted: March 16, 2016

Recall Number: Z-1076-2016

Event ID: 73008

Reason for Recall:

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

Status: Terminated

Product Quantity: 250 units

Code Information:

Catalog (Ref) # 516700 Lot numbers 5222723, 5251583 and 5253723.

Distribution Pattern:

US Distribution to:California and Utah.

Voluntary or Mandated:

Voluntary: Firm initiated