FDA Device recall Z-0288-2014
The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used fo…
- FDA Device
- Class II
- terminated
- Published 2013-11-20
On 2013-11-20 the FDA classified a Class II recall of The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used fo… 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-0288-2014 |
| 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+3 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+3 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+3 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 12618; Serial Numbers: 14040001 , 14040002 , 14040003 , 14040004 , 14040005 , 14040006 , 14040008…1) List Number 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 , 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-0288-2014%22
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