FDA Device recall Z-2726-2016
Plum A+ Infusion Pump with Hospira MedNet Software
- FDA Device
- Class II
- terminated
- Published 2016-09-14
On 2016-09-14 the FDA classified a Class II recall of Plum A+ Infusion Pump with Hospira MedNet Software by Hospira, citing the fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2726-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-02-06 |
| Published | 2016-09-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Hospira |
| Distribution | US |
Product
Plum A+ Infusion Pump with Hospira MedNet Software. List Number 20679. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor based infusion devices.
Reason
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
Identifiers
| code_info | List Number 20679. Serial numbers: 15441019, 15441020, 15441037, 15441044, 15441082, 15441093, 15441118,…List Number 20679. Serial numbers: 15441019, 15441020, 15441037, 15441044, 15441082, 15441093, 15441118, 15441226, 15441229, 15441230, 15441240, 15441241, 15441244, 15441246, 15441247, 15441249, 15441253, 15441256, 15441258, 15441260, 15441265, 15441266, 15441270, 15441271, 15441272, 15441275, 15441285, 15441303, 15441304, 15441315, 15441318, 15441321, 15441323, 15441325, 15441349, 15441350, 15441367, 15441369, 15441371, 15441372, 15441378, 15441395, 15441399, 15441405, 15441409, 15441411, 15441437, 15441458, 15441489, 15441492, 15441493, 15441502, 15441506, 15441508, 15441513, 15441515, 15441516, 15441520, 15441522, 15441524, 15441526, 15441528, 15441532, 15441533, 15441534, 15441535, 15441536, 15441554, 15441601, 15441604, 15441605, 15441610, 15441611, 15441615, 15441633, 15441637, 15441638, 15441649, 15441704, 15441765, 154 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2726-2016%22
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