FDA Device recall Z-2682-2017
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-2682-2017 |
| 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: 20679 Serial Number 15441019 15441020 15441037 15441044 15441082 15441093 15441118 15441226 1544…List number: 20679 Serial Number 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 15441803 15441816 15441839 15441942 15441960 15441966 15442037 15442062 15442090 15442124 15442126 15442157 15442193 15442197 15442207 15442235 15442 |
|---|
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-2682-2017%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.