Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hospira MedNet Medication Management Suite software Recalled by Hospira Inc., A Pfizer Company Due to Hospira MedNet 6.1 software, in combination with the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hospira Inc., A Pfizer Company directly.
Affected Products
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.
Quantity: 20
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 13 states: CT, HI, IA, ME, MA, MI, MN, NJ, NY, ND, PA, TX, WI
About Hospira Inc., A Pfizer Company
Hospira Inc., A Pfizer Company has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report