Hospira MedNet Medication Management Suite software — Class II medical device recall Z-2790-2016
Terminated recall by Hospira Inc., A Pfizer Company, reported 2016-09-21, distributed in CT, HI, IA, MA, ME, MI, MN, ND…. Hospira MedNet 6.1 software, in combination with the SapphirePlus 13.1x infusion pump, may result in incorrect
| Recall number | Z-2790-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., A Pfizer Company, Lake Forest, IL, United States |
| Recall initiated | 2016-07-28 |
| Classified | 2016-09-13 |
| Reported by FDA | 2016-09-21 |
| Terminated | 2018-11-02 |
| Distributed | CT, HI, IA, MA, ME, MI, MN, ND, NJ, NY, PA, TX, WI |
| Countries outside the US | CA |
| Quantity | 20 |
| Reason classes | software |
Product
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.
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2790-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.