Devices

Device Recall Hospira MedNet Medication Management Suite

Model / Serial
1) Software Version 5.5, List Number: 16037-04-13; 2) Software Version 5.8.1, List Number: 16037-04-31; 3) Software Version 5.8.2, List Number: 16037-04-33
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
US Nationwide in the states of FL, LA, PA, WA, WY and the country of Hong Kong
Product Description
The Hospira MedNet Medication Management Suite (MMS). || Product Usage: || The Hospira MedNet Medication Management Suite (MMS) is intended to facilitate networked communication between MMS compatible computer systems and Hospira infusion pumps. The MMS provides trained healthcare professionals with the capability to send, receive, report, and store information from interfaced external systems, and to configure and edit infusion programming parameters. The MMS is intended to provide a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data. All data entry and validation of infusion parameters is performed by a trained healthcare professional according to physicians orders.
Manufacturer
Hospira Inc.
1 Event
- Recall of Device Recall Hospira MedNet Medication Management Suite

Manufacturer

Hospira Inc.

Manufacturer Address
Hospira Inc., 275 N Field Dr, Lake Forest IL 60045-2579
Manufacturer Parent Company (2017)
Pfizer
Source
USFDA

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