FDA Device recall Z-0208-2014
Plum A+ Infusion Pump
- FDA Device
- Class II
- terminated
- Published 2013-11-20
On 2013-11-20 the FDA classified a Class II recall of Plum A+ Infusion Pump by Hospira, citing hospira has received reports of distal pressure sensor calibration drift on Plum A+ Infusers. The following error codes may be displayed during setup or infusion signifying possib….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0208-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-02-05 |
| Published | 2013-11-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Hospira |
| Distribution | US |
Product
Plum A+ Infusion Pump; List Number: 12618; Product Usage: 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
Reason
Hospira has received reports of distal pressure sensor calibration drift on Plum A+ Infusers. The following error codes may be displayed during setup or infusion signifying possible calibration drift: E180/N180, E181/N181, E186/N186, E187/N187 or E346. Additionally, if the pressure sensor calibration has drifted, users may experience false distal occlusion alarms or distal occlusions that may not
Identifiers
| code_info | List No. 12618; Serial Numbers: 14040001 , 14040002 , 14040003 , 14040004 , 14040005 , 14040006 , 14040008 , 1…List No. 12618; Serial Numbers: 14040001 , 14040002 , 14040003 , 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 , 140400 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0208-2014%22
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