FDA Device recall Z-2730-2016
Plum A+3 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+3 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-2730-2016 |
| 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+3 Infusion Pump with Hospira MedNet Software. List Number 20678. 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 20678. Serial numbers: 15541001, 15541011, 15541021, 15541031, 15541041, 15541051, 15541061, 15541071, 15…List number 20678. Serial numbers: 15541001, 15541011, 15541021, 15541031, 15541041, 15541051, 15541061, 15541071, 15541081, 15541091, 15541101, 15541111, 15541121, 15541131, 15541141, 15541151, 15541161, 15541171, 15541181, 15541191, 15541201, 15541211, 15541231, 15541241, 15541261, 15541271, 15541281, 15541291, 15541301, 15541311, 15541321, 15541331, 15541341, 15541351, 15541361, 15541371, 15541381, 15541391, 15541401, 15541411, 15541421, 15541431, 15541441, 15541451, 15541461, 15541471, 15541481, 15541491, 15541501, 15541511, 15541521, 15541531, 15541541, 15541551, 15541561, 15541571, 15541581, 15541591, 15541601, 15541611, 15541621, 15541631, 15541641, 15541651, 15541661, 15541671, 15541681, 15541691, 15541701, 15541711, 15541721, 15541731, 15541741, 15541751, 15541761, 15541771, 15541781, 15541791, 15541801, 15541811, 15541821, 15541831, 15541841, 15541851, 15541861, 15541871, 15541881, 15541891, 15541901, 15541911, 15541921, 15541931, 15541941, 15541951, 15541961, 15541971, 155 |
|---|
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-2730-2016%22
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