FDA Device recall Z-2723-2016
Plum A+ Infusion Pump
- 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 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-2723-2016 |
| 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. List Number 11971. 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 11971. Serial numbers: 13120009, 13120017, 13120018, 13120019, 13120026, 13120028, 13120037,…List Number 11971. Serial numbers: 13120009, 13120017, 13120018, 13120019, 13120026, 13120028, 13120037, 13120041, 13120042, 13120044, 13120057, 13120058, 13120068, 13120071, 13120074, 13120075, 13120082, 13120096, 13120103, 13120104, 13120107, 13120108, 13120109, 13120115, 13120128, 13120138, 13120143, 13120153, 13120160, 13120164, 13120168, 13120171, 13120174, 13120177, 13120186, 13120187, 13120200, 13120205, 13120220, 13120222, 13120223, 13120226, 13120231, 13120235, 13120237, 13120238, 13120239, 13120247, 13120248, 13120249, 13120251, 13120253, 13120262, 13120270, 13120271, 13120277, 13120279, 13120285, 13120293, 13120294, 13120295, 13120297, 13120303, 13120310, 13120311, 13120314, 13120320, 13120329, 13120343, 13120344, 13120346, 13120353, 13120354, 13120357, 13120359, 13120365, 13120366, 13120367, 13120370, 13120385, 131 |
|---|
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-2723-2016%22
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