Reported Sep 14, 2016 · Terminated
Plum A+3 Infusion Pump. List Number 12618. 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 12618. 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 12618
- serial numbers
3,257 of 3,257 codes
140400011404000214040003140400041404000514040006140400081404000914040010140400111404001214040014140400151404001614040017140400181404001914040020140400211404002214040023140400241404002514040026140400271404002714040027140400281404002814040028140400291404003014040031140400331404003414040034140400341404003514040036140400371404003814040039140400401404004114040042140400431404004414040045140400471404004814040049140400501404005114040052140400531404005414040056140400591404006114040062
- 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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