FDA Device recall Z-2728-2016
Plum A+3 Infusion Pump System
- 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 System 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-2728-2016 |
| 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 System. List Number 12348. 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 12348, Serial Numbers: 13740156, 13740256, 13740266, 13740351, 13740380, 13740451, 13740508, 13740612, 1…List number 12348, Serial Numbers: 13740156, 13740256, 13740266, 13740351, 13740380, 13740451, 13740508, 13740612, 13740632, 13740731, 13740732, 13740733, 13740734, 13740735, 13740736, 13740737, 13740738, 13740739, 13740740, 13740741, 13740742, 13740743, 13740744, 13740745, 13740746, 13740747, 13740748, 13740749, 13740750, 13740751, 13740752, 13740753, 13740754, 13740755, 13740756, 13740757, 13740758, 13740759, 13740760, 13740761, 13740762, 13740763, 13740764, 13740765, 13740766, 13740767, 13740768, 13740769, 13740770, 13740771, 13740772, 13740773, 13740774, 13740775, 13740776, 13740777, 13740778, 13740779, 13740780, 13740781, 13740782, 13740783, 13740784, 13740785, 13740786, 13740787, 13740788, 13740789, 13740790, 13740791, 13740792, 13740793, 13740794, 13740795, 13740796, 13740797, 13740798, 13740799, 13740800, 13740801, 13740802, 13740803, 13740804, 13740805, 13740806, 13740807, 13740808, 13740809, 13740810, 13740811, 13740812, 13740813, 13740814, 13740815, 13740816, 13740818, 13 |
|---|
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-2728-2016%22
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