Reported Sep 14, 2016 · Terminated

Plum A+3 Infusion Pump. List Number 12618. 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+3 Infusion Pump. List Number 12618. 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 12618
  • serial numbers

    3,257 of 3,257 codes

    • 14040001
    • 14040002
    • 14040003
    • 14040004
    • 14040005
    • 14040006
    • 14040008
    • 14040009
    • 14040010
    • 14040011
    • 14040012
    • 14040014
    • 14040015
    • 14040016
    • 14040017
    • 14040018
    • 14040019
    • 14040020
    • 14040021
    • 14040022
    • 14040023
    • 14040024
    • 14040025
    • 14040026
    • 14040027
    • 14040027
    • 14040027
    • 14040028
    • 14040028
    • 14040028
    • 14040029
    • 14040030
    • 14040031
    • 14040033
    • 14040034
    • 14040034
    • 14040034
    • 14040035
    • 14040036
    • 14040037
    • 14040038
    • 14040039
    • 14040040
    • 14040041
    • 14040042
    • 14040043
    • 14040044
    • 14040045
    • 14040047
    • 14040048
    • 14040049
    • 14040050
    • 14040051
    • 14040052
    • 14040053
    • 14040054
    • 14040056
    • 14040059
    • 14040061
    • 14040062
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.

Free recall alerts

Get alerted about new Hospira Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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, 5:20 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.