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

    • 12570148
    • 12570150
    • 12570154
    • 12570163
    • 12570170
    • 12570177
    • 12570204
    • 12570211
    • 12570212
    • 12570255
    • 12570270
    • 12570319
    • 12570359
    • 12570385
    • 12570413
    • 12570425
    • 12570455
    • 12570487
    • 12570662
    • 12570695
    • 12570854
    • 12570915
    • 12571080
    • 12571243
    • 12571437
    • 12571631
    • 12571692
    • 12571776
    • 12571826
    • 12571835
    • 12571837
    • 12571842
    • 12571877
    • 12571880
    • 12571886
    • 12572317
    • 12572369
    • 12572586
    • 12572909
    • 12573547
    • 12573567
    • 12573837
    • 12573990
    • 12574424
    • 12574501
    • 12574524
    • 12574556
    • 12574599
    • 12574619
    • 12574731
    • 12574749
    • 12574853
    • 12574858
    • 12574860
    • 12574865
    • 12574961
    • 12575626
    • 12575698
    • 12575886
    • 12576125
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.

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.

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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, 5:25 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.