Reported Sep 14, 2016 · Terminated

Plum A+3 Infusion Pump System. List Number 12348. The Plum A+ Infusion Systems are a multi-purpose family of devices…

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 System. List Number 12348. 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 12348
  • Serial Numbers

    214 of 214 codes

    • 13740156
    • 13740256
    • 13740266
    • 13740351
    • 13740380
    • 13740451
    • 13740508
    • 13740612
    • 13740632
    • 13740731
    • 13740732
    • 13740733
    • 13740734
    • 13740735
    • 13740736
    • 13740737
    • 13740738
    • 13740739
    • 13740740
    • 13740741
    • 13740742
    • 13740743
    • 13740744
    • 13740745
    • 13740746
    • 13740747
    • 13740748
    • 13740749
    • 13740750
    • 13740751
    • 13740752
    • 13740753
    • 13740754
    • 13740755
    • 13740756
    • 13740757
    • 13740758
    • 13740759
    • 13740760
    • 13740761
    • 13740762
    • 13740763
    • 13740764
    • 13740765
    • 13740766
    • 13740767
    • 13740768
    • 13740769
    • 13740770
    • 13740771
    • 13740772
    • 13740773
    • 13740774
    • 13740775
    • 13740776
    • 13740777
    • 13740778
    • 13740779
    • 13740780
    • 13740781
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, 4:45 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.