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 number20679 Serial Number

    3,257 of 3,257 codes

    • 15441019
    • 15441020
    • 15441037
    • 15441044
    • 15441082
    • 15441093
    • 15441118
    • 15441226
    • 15441229
    • 15441230
    • 15441240
    • 15441241
    • 15441244
    • 15441246
    • 15441247
    • 15441249
    • 15441253
    • 15441256
    • 15441258
    • 15441260
    • 15441265
    • 15441266
    • 15441270
    • 15441271
    • 15441272
    • 15441275
    • 15441285
    • 15441303
    • 15441304
    • 15441315
    • 15441318
    • 15441321
    • 15441323
    • 15441325
    • 15441349
    • 15441350
    • 15441367
    • 15441369
    • 15441371
    • 15441372
    • 15441378
    • 15441395
    • 15441399
    • 15441405
    • 15441409
    • 15441411
    • 15441437
    • 15441458
    • 15441489
    • 15441492
    • 15441493
    • 15441502
    • 15441506
    • 15441508
    • 15441513
    • 15441515
    • 15441516
    • 15441520
    • 15441522
    • 15441524
Amount recalled
7351 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, 4:49 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.