FDAFDA · Food and drugs·Recall number Z-2790-2016
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.
Published September 21, 2016 · Recall initiated: July 28, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc., A Pfizer Company
- Distributor
- Worldwide Distribution - US including ND, TX, MI, MN, WI, IA, ME, HI, PA, MA, NJ, NY, CT, and Internationally to Canada.
- Lot
- List Numbers 16037-64-02 and 16037-64-03
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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