FDA Device recall Z-2679-2017
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-2679-2017 |
| 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: 12391 Serial Number 13840001 13840002 13840003 13840004 13840005 13840006 13840007 13840008 1384…List number: 12391 Serial Number 13840001 13840002 13840003 13840004 13840005 13840006 13840007 13840008 13840009 13840010 13840011 13840012 13840013 13840014 13840015 13840016 13840017 13840018 13840019 13840020 13840021 13840022 13840023 13840024 13840025 13840026 13840027 13840028 13840029 13840030 13840031 13840032 13840033 13840034 13840035 13840036 13840037 13840038 13840039 13840040 13840041 13840042 13840043 13840044 13840045 13840046 13840047 13840048 13840049 13840050 13840051 13840052 13840053 13840054 13840055 13840056 13840057 13840058 13840059 13840060 13840061 13840062 13840063 13840064 13840065 13840066 13840067 13840068 13840069 13840070 13840071 13840072 13840073 13840074 13840075 13840076 13840077 13840078 13840079 13840080 13840081 13840082 13840083 13840084 13840085 13840086 13840087 13840088 13840089 13840090 13840091 13840092 13840093 13840094 13840095 13840096 13840 |
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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-2679-2017%22
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