Reported Nov 20, 2013 · Terminated
The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines in and one line…
Hospira Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hospira Inc. · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
- 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.
- Lot codes and dates
- 1) List Number 20678
- Serial Numbers
2,714 of 2,714 codes
155410011554101115541021155410311554104115541051155410611554107115541081155410911554110115541111155411211554113115541141155411511554116115541171155411811554119115541201155412111554123115541241155412611554127115541281155412911554130115541311155413211554133115541341155413511554136115541371155413811554139115541401155414111554142115541431155414411554145115541461155414711554148115541491155415011554151115541521155415311554154115541551155415611554157115541581155415911554160115541611
- Amount recalled
- 21,551 units
This recall covers 15 products
The agency filed one notice per product. You are reading one of them; the other 14 are below.
2 more are in the archive.
Where it was sold
Why it was recalled
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
This product could cause temporary or reversible health problems — stop using it.
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