Reported Sep 14, 2016 · Terminated
Plum A+3 Infusion Pump. List Number 12391. The Plum A+ Infusion Systems are a multi-purpose family of devices that…
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?
- Plum A+3 Infusion Pump. List Number 12391. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor based infusion devices.
- Lot codes and dates
- List Number 12391
- Serial numbers
2,714 of 2,714 codes
138400011384000213840003138400041384000513840006138400071384000813840009138400101384001113840012138400131384001413840015138400161384001713840018138400191384002013840021138400221384002313840024138400251384002613840027138400281384002913840030138400311384003213840033138400341384003513840036138400371384003813840039138400401384004113840042138400431384004413840045138400461384004713840048138400491384005013840051138400521384005313840054138400551384005613840057138400581384005913840060
- Amount recalled
- 357,778 total
This recall covers 9 products
The agency filed one notice per product. You are reading one of them; the other 8 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
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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