Reported Sep 14, 2016 · Terminated
Plum A+ Infusion Pump. List Number 11973. 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+ Infusion Pump. List Number 11973. 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 11973
- Serial numbers
71 of 71 codes
125701481257015012570154125701631257017012570177125702041257021112570212125702551257027012570319125703591257038512570413125704251257045512570487125706621257069512570854125709151257108012571243125714371257163112571692125717761257182612571835125718371257184212571877125718801257188612572317125723691257258612572909125735471257356712573837125739901257442412574501125745241257455612574599125746191257473112574749125748531257485812574860125748651257496112575626125756981257588612576125
- 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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