FDA Device recall Z-2683-2017
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-2683-2017 |
| 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: 20792 Serial Number 16061001 16061002 16061003 16061004 16061005 16061006 16061007 16061008 1606…List number: 20792 Serial Number 16061001 16061002 16061003 16061004 16061005 16061006 16061007 16061008 16061009 16061010 16061011 16061012 16061013 16061014 16061015 16061016 16061017 16061018 16061019 16061020 16061021 16061022 16061023 16061025 16061026 16061027 16061028 16061029 16061030 16061031 16061032 16061033 16061034 16061035 16061036 16061037 16061038 16061039 16061040 16061041 16061042 16061043 16061044 16061045 16061046 16061047 16061048 16061049 16061050 16061051 16061052 16061053 16061054 16061055 16061056 16061057 16061058 16061059 16061060 16061061 16061062 16061063 16061064 16061065 16061066 16061067 16061068 16061069 16061070 16061071 16061072 16061073 16061074 16061075 16061076 16061077 16061078 16061079 16061080 16061081 16061082 16061083 16061084 16061085 16061086 16061087 16061088 16061089 16061090 16061091 16061092 16061093 16061094 16061095 16061096 16061097 16061 |
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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-2683-2017%22
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