FDA Device recall Z-0290-2014
The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for…
- FDA Device
- Class II
- terminated
- Published 2013-11-20
On 2013-11-20 the FDA classified a Class II recall of The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for… by Hospira, citing plum A+ infusers have the potential for the distal (occlusion) press sensor pin to break. The distal pressure sensor pin is a part of the overall subsystem that measures the press….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0290-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-02-01 |
| Published | 2013-11-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Hospira |
| Distribution | US |
Product
The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+ Infusion System is designed to deliver parenteral, enteral, or epidural infusions over a broad range of infusion rates from multiple fluid container types. The Plum A+ Infusion System includes an infuser, disposable IV sets (hereafter called a set), optional accessories, and this operator's manual. The Plum A+ Infusion System with Hospira MedNet Software is indicated for use in parenteral, enteral and epidural therapies and the administration of whole blood and blood products.
Reason
Plum A+ infusers have the potential for the distal (occlusion) press sensor pin to break. The distal pressure sensor pin is a part of the overall subsystem that measures the pressure within the distal line of the administration set and indicates the presence of a full or partial distal occlusion. A broken distal pin can only be detected via a visual inspection of the distal pressure pin. A broken
Identifiers
| code_info | *** 1) List Number 20679; Serial Numbers: 15441019 , 15441020 , 15441037 , 15441044 , 15441082 , 15441093 , 15441…*** 1) List Number 20679; Serial Numbers: 15441019 , 15441020 , 15441037 , 15441044 , 15441082 , 15441093 , 15441118 , 15441226 , 15441229 , 15441230 , 15441240 , 15441241 , 15441244 , 15441246 , 15441247 , 15441249 , 15441253 , 15441256 , 15441258 , 15441260 , 15441265 , 15441266 , 15441270 , 15441271 , 15441272 , 15441275 , 15441285 , 15441303 , 15441304 , 15441315 , 15441318 , 15441321 , 15441323 , 15441325 , 15441349 , 15441350 , 15441367 , 15441369 , 15441371 , 15441372 , 15441378 , 15441395 , 15441399 , 15441405 , 15441409 , 15441411 , 15441437 , 15441458 , 15441489 , 15441492 , 15441493 , 15441502 , 15441506 , 15441508 , 15441513 , 15441515 , 15441516 , 15441520 , 15441522 , 15441524 , 15441526 , 15441528 , 15441532 , 15441533 , 15441534 , 15441535 , 15441536 , 15441554 , 15441601 , 15441604 , 15441605 , 15441610 , 15441611 , 15441615 , 15441633 , 15441637 , 15441638 , 15441649 , 15441704 , 15441765 , |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0290-2014%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.