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

    • 15541001
    • 15541011
    • 15541021
    • 15541031
    • 15541041
    • 15541051
    • 15541061
    • 15541071
    • 15541081
    • 15541091
    • 15541101
    • 15541111
    • 15541121
    • 15541131
    • 15541141
    • 15541151
    • 15541161
    • 15541171
    • 15541181
    • 15541191
    • 15541201
    • 15541211
    • 15541231
    • 15541241
    • 15541261
    • 15541271
    • 15541281
    • 15541291
    • 15541301
    • 15541311
    • 15541321
    • 15541331
    • 15541341
    • 15541351
    • 15541361
    • 15541371
    • 15541381
    • 15541391
    • 15541401
    • 15541411
    • 15541421
    • 15541431
    • 15541441
    • 15541451
    • 15541461
    • 15541471
    • 15541481
    • 15541491
    • 15541501
    • 15541511
    • 15541521
    • 15541531
    • 15541541
    • 15541551
    • 15541561
    • 15541571
    • 15541581
    • 15541591
    • 15541601
    • 15541611
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.

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, 6:51 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.