Reported Mar 2, 2016 · Terminated

The Symbiq infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled…

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?

  • The Symbiq infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. It is intended primarily for use in the hospital setting and can be used in other acute and non-acute areas, such as, but not limited to, Nursing Homes, Mobile Intensive Care, Ambulatory Infusion, Centers, Hospice, Sub acute facilities, Outpatient/Surgical Centers, Long-term Care, Urgent Care, Transport, and Physician Offices.
Lot codes and dates
  • Lot Code 16026 &16027
  • with the following serial numbers

    3,255 of 3,255 codes

    • 14339221
    • 14339224
    • 14339232
    • 14339261
    • 14339275
    • 14339296
    • 14339308
    • 14339321
    • 14339335
    • 14339349
    • 14339353
    • 14339357
    • 14339371
    • 14339372
    • 14339378
    • 14339387
    • 14339391
    • 14339396
    • 14339401
    • 14339504
    • 14339515
    • 14339553
    • 14339710
    • 14339719
    • 14339725
    • 14339733
    • 14339738
    • 14339742
    • 14339748
    • 14339761
    • 14339769
    • 14339771
    • 14339799
    • 14339815
    • 14339822
    • 14339851
    • 14339887
    • 14339888
    • 14339904
    • 14339913
    • 14339964
    • 14339989
    • 14339998
    • 14339999
    • 14340001
    • 14340014
    • 14340041
    • 14340042
    • 14340069
    • 14340070
    • 14340071
    • 14340094
    • 14340096
    • 14340110
    • 14340117
    • 14340119
    • 14340120
    • 14340122
    • 14340123
    • 14340124
Amount recalled
6634 units.

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Potential for the Symbiq pole clamp assemblies to be missing the rubber stop pad.

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 28, 2016 · Data as of Sep 19, 6:01 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.