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 number 11971; Serial Numbers

    3,257 of 3,257 codes

    • 13120009
    • 13120017
    • 13120018
    • 13120019
    • 13120026
    • 13120028
    • 13120037
    • 13120041
    • 13120042
    • 13120044
    • 13120057
    • 13120058
    • 13120068
    • 13120071
    • 13120074
    • 13120075
    • 13120082
    • 13120096
    • 13120103
    • 13120104
    • 13120107
    • 13120108
    • 13120109
    • 13120115
    • 13120128
    • 13120138
    • 13120143
    • 13120153
    • 13120160
    • 13120164
    • 13120168
    • 13120171
    • 13120174
    • 13120177
    • 13120186
    • 13120187
    • 13120200
    • 13120205
    • 13120220
    • 13120222
    • 13120223
    • 13120226
    • 13120231
    • 13120235
    • 13120237
    • 13120238
    • 13120239
    • 13120247
    • 13120248
    • 13120249
    • 13120251
    • 13120253
    • 13120262
    • 13120270
    • 13120271
    • 13120277
    • 13120279
    • 13120285
    • 13120293
    • 13120294
Amount recalled
10609 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, 5:21 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.