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 number12618 Serial Number
3,257 of 3,257 codes
140400011404000214040004140400051404000614040008140400091404001014040011140400121404001414040015140400161404001714040018140400191404002014040021140400221404002314040024140400251404002614040027140400271404002714040028140400281404002814040029140400301404003114040033140400341404003414040034140400351404003614040037140400381404003914040040140400411404004214040043140400441404004514040047140400481404004914040050140400511404005214040053140400541404005614040059140400611404006214040063
- List number12618 Serial Number
- Amount recalled
- 7848 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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