FDA Device recall Z-0287-2014
The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for…
- FDA Device
- Class II
- terminated
- Published 2013-11-20
On 2013-11-20 the FDA classified a Class II recall of The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for… by Hospira, citing plum A+ infusers have the potential for the distal (occlusion) press sensor pin to break. The distal pressure sensor pin is a part of the overall subsystem that measures the press….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0287-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-02-01 |
| Published | 2013-11-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Hospira |
| Distribution | US |
Product
The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+ Infusion System is designed to deliver parenteral, enteral, or epidural infusions over a broad range of infusion rates from multiple fluid container types. The Plum A+ Infusion System includes an infuser, disposable IV sets (hereafter called a set), optional accessories, and this operator's manual. The Plum A+ Infusion System with Hospira MedNet Software is indicated for use in parenteral, enteral and epidural therapies and the administration of whole blood and blood products.
Reason
Plum A+ infusers have the potential for the distal (occlusion) press sensor pin to break. The distal pressure sensor pin is a part of the overall subsystem that measures the pressure within the distal line of the administration set and indicates the presence of a full or partial distal occlusion. A broken distal pin can only be detected via a visual inspection of the distal pressure pin. A broken
Identifiers
| code_info | 1) List Number 12391; Serial Numbers: 13840001 , 13840002 , 13840003 , 13840004 , 13840005 , 13840006 , 13840007…1) List Number 12391; Serial Numbers: 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 , 1 |
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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-0287-2014%22
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