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 number11005
  • Serial Numbers

    180 of 180 codes

    • 16792201
    • 16792202
    • 16792205
    • 16792206
    • 16792208
    • 16792209
    • 16792210
    • 16792211
    • 16792213
    • 16792216
    • 16792217
    • 16792219
    • 16792220
    • 16792222
    • 16792223
    • 16792224
    • 16792225
    • 16792226
    • 16792227
    • 16792228
    • 16792230
    • 16792232
    • 16792233
    • 16792234
    • 16792235
    • 16792236
    • 16792238
    • 16792239
    • 16792240
    • 16792241
    • 16792242
    • 16792244
    • 16792245
    • 16792246
    • 16792248
    • 16792249
    • 16792250
    • 16792251
    • 16792252
    • 16792253
    • 16792254
    • 16792255
    • 16792256
    • 16792257
    • 16792258
    • 16792259
    • 16792260
    • 16792261
    • 16792263
    • 16792264
    • 16792265
    • 16792266
    • 16792268
    • 16792269
    • 16792271
    • 16792272
    • 16792273
    • 18807402
    • 18807405
    • 18807406
Amount recalled
180 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, 5:19 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.