FDA Device recall Z-2675-2017
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-2675-2017 |
| 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: 11005; Serial Numbers: 16792201 16792202 16792205 16792206 16792208 16792209 16792210 16792211…List number: 11005; Serial Numbers: 16792201 16792202 16792205 16792206 16792208 16792209 16792210 16792211 16792213 16792216 16792217 16792219 16792220 16792222 16792223 16792224 16792225 16792226 16792227 16792228 16792230 16792232 16792233 16792234 16792235 16792236 16792238 16792239 16792240 16792241 16792242 16792244 16792245 16792246 16792248 16792249 16792250 16792251 16792252 16792253 16792254 16792255 16792256 16792257 16792258 16792259 16792260 16792261 16792263 16792264 16792265 16792266 16792268 16792269 16792271 16792272 16792273 18807402 18807405 18807406 18807407 18807408 18807409 18807410 18807413 18807414 18807417 18807418 18807420 18807421 18807423 18807427 18807428 18807429 18807430 18807431 18807432 18807433 18807434 18807439 18807443 18807444 18807446 18807449 18807452 18807453 18807455 18807456 18807459 18807463 18807466 18807472 18807474 18807478 18807484 18807485 1 |
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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-2675-2017%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.