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 number20792 Serial Number

    3,257 of 3,257 codes

    • 16061001
    • 16061002
    • 16061003
    • 16061004
    • 16061005
    • 16061006
    • 16061007
    • 16061008
    • 16061009
    • 16061010
    • 16061011
    • 16061012
    • 16061013
    • 16061014
    • 16061015
    • 16061016
    • 16061017
    • 16061018
    • 16061019
    • 16061020
    • 16061021
    • 16061022
    • 16061023
    • 16061025
    • 16061026
    • 16061027
    • 16061028
    • 16061029
    • 16061030
    • 16061031
    • 16061032
    • 16061033
    • 16061034
    • 16061035
    • 16061036
    • 16061037
    • 16061038
    • 16061039
    • 16061040
    • 16061041
    • 16061042
    • 16061043
    • 16061044
    • 16061045
    • 16061046
    • 16061047
    • 16061048
    • 16061049
    • 16061050
    • 16061051
    • 16061052
    • 16061053
    • 16061054
    • 16061055
    • 16061056
    • 16061057
    • 16061058
    • 16061059
    • 16061060
    • 16061061
Amount recalled
363892 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.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Icu recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 31, 2018 · Data as of Sep 19, 5:28 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.