Reported Nov 20, 2013 · Terminated
The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out…
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+ 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.
- Lot codes and dates
- 1) List Number 12391
- Serial Numbers
2,714 of 2,714 codes
138400011384000213840003138400041384000513840006138400071384000813840009138400101384001113840012138400131384001413840015138400161384001713840018138400191384002013840021138400221384002313840024138400251384002613840027138400281384002913840030138400311384003213840033138400341384003513840036138400371384003813840039138400401384004113840042138400431384004413840045138400461384004713840048138400491384005013840051138400521384005313840054138400551384005613840057138400581384005913840060
- Amount recalled
- 182,971 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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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