FDA Device recall Z-2725-2016
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-2725-2016 |
| 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 12391. 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 12391. Serial numbers: 13840001, 13840002, 13840003, 13840004, 13840005, 13840006, 13840007,…List Number 12391. Serial numbers: 13840001, 13840002, 13840003, 13840004, 13840005, 13840006, 13840007, 13840008, 13840009, 13840010, 13840011, 13840012, 13840013, 13840014, 13840015, 13840016, 13840017, 13840018, 13840019, 13840020, 13840021, 13840022, 13840023, 13840024, 13840025, 13840026, 13840027, 13840028, 13840029, 13840030, 13840031, 13840032, 13840033, 13840034, 13840035, 13840036, 13840037, 13840038, 13840039, 13840040, 13840041, 13840042, 13840043, 13840044, 13840045, 13840046, 13840047, 13840048, 13840049, 13840050, 13840051, 13840052, 13840053, 13840054, 13840055, 13840056, 13840057, 13840058, 13840059, 13840060, 13840061, 13840062, 13840063, 13840064, 13840065, 13840066, 13840067, 13840068, 13840069, 13840070, 13840071, 13840072, 13840073, 13840074, 13840075, 13840076, 13840077, 13840078, 13840079, 13840080, 138 |
|---|
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-2725-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.