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 number20678 Serial Number
3,257 of 3,257 codes
155410011554101115541021155410311554104115541051155410611554107115541081155410911554110115541111155411211554113115541141155411511554116115541171155411811554119115541201155412111554123115541241155412611554127115541281155412911554130115541311155413211554133115541341155413511554136115541371155413811554139115541401155414111554142115541431155414411554145115541461155414711554148115541491155415011554151115541521155415311554154115541551155415611554157115541581155415911554160115541611
- List number20678 Serial Number
- Amount recalled
- 21703 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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