Reported Sep 14, 2016 · Terminated
Plum A+3 Infusion Pump with Hospira MedNet Software. List Number 20678. The Plum A+ Infusion Systems are a…
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 with Hospira MedNet Software. List Number 20678. 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 20678
- Serial numbers
3,257 of 3,257 codes
155410011554101115541021155410311554104115541051155410611554107115541081155410911554110115541111155411211554113115541141155411511554116115541171155411811554119115541201155412111554123115541241155412611554127115541281155412911554130115541311155413211554133115541341155413511554136115541371155413811554139115541401155414111554142115541431155414411554145115541461155414711554148115541491155415011554151115541521155415311554154115541551155415611554157115541581155415911554160115541611
- 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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