Reported Aug 7, 2013 · Terminated

The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals,…

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 Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and blood products via parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural, or irrigation routes of administration.
Lot codes and dates
  • *** 1) List Number 16206
  • Serial Numbers

    1,195 of 1,195 codes

    • 0017234975
    • 0017234978
    • 0017234979
    • 0017234980
    • 0017234981
    • 0017234982
    • 0017234983
    • 0017234984
    • 0017234985
    • 0017234986
    • 0017234988
    • 0017234991
    • 0017234992
    • 0017234993
    • 0017234994
    • 0017234995
    • 0017234996
    • 0017234997
    • 0017234998
    • 0017234999
    • 0017235001
    • 0017235002
    • 0017235003
    • 0017235004
    • 0017235005
    • 0017235006
    • 0017235007
    • 0017235008
    • 0017235009
    • 0017235010
    • 0017235011
    • 0017235014
    • 0017235015
    • 0017235016
    • 0017235017
    • 0017235018
    • 0017235019
    • 0017235020
    • 0017235021
    • 0017235022
    • 0017235023
    • 0017235024
    • 0017235025
    • 0017235026
    • 0017235028
    • 0017235029
    • 0017235030
    • 0017235031
    • 0017235032
    • 0017235033
    • 0017235034
    • 0017235035
    • 0017235036
    • 0017235037
    • 0017235038
    • 0017235039
    • 0017235041
    • 0017235042
    • 0017235043
    • 0017235044
  • Serial Numbers

    1,129 of 1,129 codes

    • 0017330766
    • 0017330767
    • 0017330769
    • 0017330778
    • 0017330784
    • 0017330786
    • 0017330789
    • 0017330790
    • 0017330791
    • 0017330805
    • 0017330808
    • 0017330809
    • 0017330811
    • 0017330812
    • 0017330813
    • 0017330814
    • 0017330816
    • 0017330817
    • 0017330819
    • 0017330822
    • 0017330823
    • 0017330826
    • 0017330827
    • 0017330829
    • 0017330830
    • 0017330831
    • 0017330833
    • 0017330835
    • 0017330836
    • 0017330838
    • 0017330839
    • 0017330840
    • 0017330841
    • 0017330843
    • 0017330844
    • 0017330845
    • 0017330846
    • 0017330848
    • 0017330851
    • 0017330852
    • 0017330853
    • 0017330854
    • 0017330855
    • 0017330857
    • 0017330859
    • 0017330866
    • 0017330872
    • 0017330873
    • 0017330875
    • 0017330876
    • 0017330877
    • 0017330878
    • 0017330880
    • 0017330881
    • 0017330884
    • 0017330885
    • 0017330886
    • 0017330887
    • 0017330889
    • 0017330892
Amount recalled
2,791 units

Where it was sold

Why it was recalled

The devices secondary audio signal fails to activate.

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 7, 2016 · Data as of Sep 19, 5:31 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.