Reported Jul 19, 2017 · Terminated
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies…
Icu
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: ICU · 600 N Field Dr · Lake Forest, IL · 60045-4835
Is this the product you have?
- The Plum A+ Infusion Systems are a multipurpose 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. The pumps are available in single channel and in triple channel pumping mechanism types.
- Lot codes and dates
- List number11973 Serial Numbers
71 of 71 codes
125701481257015012570154125701631257017012570177125702041257021112570212125702551257027012570319125703591257038512570413125704251257045512570487125706621257069512570854125709151257108012571243125714371257163112571692125717761257182612571835125718371257184212571877125718801257188612572317125723691257258612572909125735471257356712573837125739901257442412574501125745241257455612574599125746191257473112574749125748531257485812574860125748651257496112575626125756981257588612576125
- List number11973 Serial Numbers
- Amount recalled
- 71 units
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
Why it was recalled
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
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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