FDA Device recall Z-2676-2017
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-2676-2017 |
| 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 11971; Serial Numbers 13120009 13120017 13120018 13120019 13120026 13120028 13120037 13120041 13…List number 11971; Serial Numbers 13120009 13120017 13120018 13120019 13120026 13120028 13120037 13120041 13120042 13120044 13120057 13120058 13120068 13120071 13120074 13120075 13120082 13120096 13120103 13120104 13120107 13120108 13120109 13120115 13120128 13120138 13120143 13120153 13120160 13120164 13120168 13120171 13120174 13120177 13120186 13120187 13120200 13120205 13120220 13120222 13120223 13120226 13120231 13120235 13120237 13120238 13120239 13120247 13120248 13120249 13120251 13120253 13120262 13120270 13120271 13120277 13120279 13120285 13120293 13120294 13120295 13120297 13120303 13120310 13120311 13120314 13120320 13120329 13120343 13120344 13120346 13120353 13120354 13120357 13120359 13120365 13120366 13120367 13120370 13120385 13120390 13120391 13120394 13120399 13120401 13120405 13120419 13120422 13120424 13120440 13120441 13120452 13120460 13120462 13120467 13120472 131 |
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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-2676-2017%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.