FDA Device recall Z-2727-2016
Plum A+ 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+ 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-2727-2016 |
| 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 with Hospira MedNet Software. List Number 20792. 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 20792. Serial numbers: 16061001, 16061002, 16061003, 16061004, 16061005, 16061006, 16061007,…List Number 20792. Serial numbers: 16061001, 16061002, 16061003, 16061004, 16061005, 16061006, 16061007, 16061008, 16061009, 16061010, 16061011, 16061012, 16061013, 16061014, 16061015, 16061016, 16061017, 16061018, 16061019, 16061020, 16061021, 16061022, 16061023, 16061025, 16061026, 16061027, 16061028, 16061029, 16061030, 16061031, 16061032, 16061033, 16061034, 16061035, 16061036, 16061037, 16061038, 16061039, 16061040, 16061041, 16061042, 16061043, 16061044, 16061045, 16061046, 16061047, 16061048, 16061049, 16061050, 16061051, 16061052, 16061053, 16061054, 16061055, 16061056, 16061057, 16061058, 16061059, 16061060, 16061061, 16061062, 16061063, 16061064, 16061065, 16061066, 16061067, 16061068, 16061069, 16061070, 16061071, 16061072, 16061073, 16061074, 16061075, 16061076, 16061077, 16061078, 16061079, 16061080, 16061081, 160 |
|---|
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-2727-2016%22
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