FDA Device recall Z-2681-2017
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general s…
- FDA Device
- Class II
- terminated
- Published 2017-07-19
On 2017-07-19 the FDA classified a Class II recall of The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general s… by Icu, citing A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2681-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-02-01 |
| Published | 2017-07-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Icu |
| Distribution | US |
Product
The Plum A+ Infusion Systems are a multipurpose 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. The pumps are available in single channel and in triple channel pumping mechanism types.
Reason
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
Identifiers
| code_info | List number: 20678 Serial Number 15541001 15541011 15541021 15541031 15541041 15541051 15541061 15541071 1554…List number: 20678 Serial Number 15541001 15541011 15541021 15541031 15541041 15541051 15541061 15541071 15541081 15541091 15541101 15541111 15541121 15541131 15541141 15541151 15541161 15541171 15541181 15541191 15541201 15541211 15541231 15541241 15541261 15541271 15541281 15541291 15541301 15541311 15541321 15541331 15541341 15541351 15541361 15541371 15541381 15541391 15541401 15541411 15541421 15541431 15541441 15541451 15541461 15541471 15541481 15541491 15541501 15541511 15541521 15541531 15541541 15541551 15541561 15541571 15541581 15541591 15541601 15541611 15541621 15541631 15541641 15541651 15541661 15541671 15541681 15541691 15541701 15541711 15541721 15541731 15541741 15541751 15541761 15541771 15541781 15541791 15541801 15541811 15541821 15541831 15541841 15541851 15541861 15541871 15541881 15541891 15541901 15541911 15541921 15541931 15541941 15541951 15541961 15541971 15541 |
|---|
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-2681-2017%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.