Reported Sep 14, 2016 · Terminated

Plum A+3 Infusion Pump with Hospira MedNet Software. List Number 20678. The Plum A+ Infusion Systems are a…

Hospira Inc.

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: Hospira Inc. · 275 N Field Dr · Lake Forest, IL · 60045-2579

Is this the product you have?

  • Plum A+3 Infusion Pump with Hospira MedNet Software. List Number 20678. The Plum A+ Infusion Systems are a multi-purpose 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.
Lot codes and dates
  • List number 20678
  • Serial numbers

    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
357,778 total

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
  • PR

Why it was recalled

The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.

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 Nov 14, 2016 · Data as of Sep 19, 6:02 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.