FDA Device recall Z-2680-2017
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-2680-2017 |
| 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: 12618 Serial Number 14040001 14040002 14040004 14040005 14040006 14040008 14040009 14040010 1404…List number: 12618 Serial Number 14040001 14040002 14040004 14040005 14040006 14040008 14040009 14040010 14040011 14040012 14040014 14040015 14040016 14040017 14040018 14040019 14040020 14040021 14040022 14040023 14040024 14040025 14040026 14040027 14040027 14040027 14040028 14040028 14040028 14040029 14040030 14040031 14040033 14040034 14040034 14040034 14040035 14040036 14040037 14040038 14040039 14040040 14040041 14040042 14040043 14040044 14040045 14040047 14040048 14040049 14040050 14040051 14040052 14040053 14040054 14040056 14040059 14040061 14040062 14040063 14040064 14040065 14040066 14040067 14040068 14040069 14040070 14040071 14040072 14040073 14040074 14040075 14040076 14040077 14040078 14040079 14040080 14040081 14040082 14040083 14040084 14040085 14040086 14040087 14040088 14040089 14040090 14040091 14040092 14040093 14040094 14040095 14040096 14040097 14040098 14040099 14040 |
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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-2680-2017%22
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