Reported Sep 14, 2016 · Terminated

Plum A+ Infusion Pump. List Number 11971. The Plum A+ Infusion Systems are a multi-purpose family of devices that…

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+ Infusion Pump. List Number 11971. 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 11971
  • Serial numbers

    2,714 of 2,714 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
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.

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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, 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.