Hospira Inc., A Pfizer Company: Medical Device Recall in 2016 - (Recall #: Z-2790-2016)

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:

Hospira MedNet Medication Management Suite software, version 6.1, List Numbers 16037-64-02 and 16037-64-03, in combination with the SapphirePlus 13.1x infusion pump Hospira MedNet Medication Management Suite is intended to facilitate networked communication between compatible computer systems and Hospital infusion pumps.

Product Classification:

Class II

Date Initiated: July 28, 2016

Date Posted: September 21, 2016

Recall Number: Z-2790-2016

Event ID: 74903

Reason for Recall:

Hospira MedNet 6.1 software, in combination with the SapphirePlus 13.1x infusion pump, may result in incorrect bolus amount calculations for drugs whose concentrations are listed in Million Units.

Status: Terminated

Product Quantity: 20

Code Information:

List Numbers 16037-64-02 and 16037-64-03

Distribution Pattern:

Worldwide Distribution - US including ND, TX, MI, MN, WI, IA, ME, HI, PA, MA, NJ, NY, CT, and Internationally to Canada.

Voluntary or Mandated:

Voluntary: Firm initiated