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 20679
- Serial Numbers
2,714 of 2,714 codes
154410191544102015441037154410441544108215441093154411181544122615441229154412301544124015441241154412441544124615441247154412491544125315441256154412581544126015441265154412661544127015441271154412721544127515441285154413031544130415441315154413181544132115441323154413251544134915441350154413671544136915441371154413721544137815441395154413991544140515441409154414111544143715441458154414891544149215441493154415021544150615441508154415131544151515441516154415201544152215441524
- Amount recalled
- 1) List Number 20679: 7,737 units; 2) List Number 20792:
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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