FDA Device recall Z-2729-2016
Plum A+3 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+3 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-2729-2016 |
| 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. List Number 12618. 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 12618. serial numbers: 14040001, 14040002, 14040003, 14040004, 14040005, 14040006, 14040008, 14040009, 140…list number 12618. serial numbers: 14040001, 14040002, 14040003, 14040004, 14040005, 14040006, 14040008, 14040009, 14040010, 14040011, 14040012, 14040014, 14040015, 14040016, 14040017, 14040018, 14040019, 14040020, 14040021, 14040022, 14040023, 14040024, 14040025, 14040026, 14040027, 14040027, 14040027, 14040028, 14040028, 14040028, 14040029, 14040030, 14040031, 14040033, 14040034, 14040034, 14040034, 14040035, 14040036, 14040037, 14040038, 14040039, 14040040, 14040041, 14040042, 14040043, 14040044, 14040045, 14040047, 14040048, 14040049, 14040050, 14040051, 14040052, 14040053, 14040054, 14040056, 14040059, 14040061, 14040062, 14040063, 14040064, 14040065, 14040066, 14040067, 14040068, 14040069, 14040070, 14040071, 14040072, 14040073, 14040074, 14040075, 14040076, 14040077, 14040078, 14040079, 14040080, 14040081, 14040082, 14040083, 14040084, 14040085, 14040086, 14040087, 14040088, 14040089, 14040090, 14040091, 14040092, 14040093, 14040094, 14040095, 14040096, 14040097, 14040098, 1404 |
|---|
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-2729-2016%22
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