Reported Nov 2, 2016 · Terminated

Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Device is a general…

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?

  • Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Device is a general purpose infusion pump designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes, blood and blood products for parenteral administration; and various solution through enteral, intravenous, intra-arterial, subcutaneous, and pathways.
Lot codes and dates
  • 3,260 of 3,260 codes

    • 14589003
    • 14589008
    • 14589009
    • 14589012
    • 14589013
    • 14589014
    • 14589015
    • 14589017
    • 14589020
    • 14589022
    • 14589028
    • 14589030
    • 14589031
    • 14589033
    • 14589034
    • 14589035
    • 14589043
    • 14589046
    • 14589048
    • 14589049
    • 14589050
    • 14589053
    • 14589057
    • 14589060
    • 14589063
    • 14589064
    • 14589066
    • 14589068
    • 14589072
    • 14589078
    • 14589082
    • 14589083
    • 14589086
    • 14589092
    • 14589095
    • 14589100
    • 14589101
    • 14589105
    • 14589108
    • 14589110
    • 14589111
    • 14589116
    • 14589117
    • 14589118
    • 14589121
    • 14589127
    • 14589131
    • 14589133
    • 14589135
    • 14589136
    • 14589137
    • 14589139
    • 14589140
    • 14589141
    • 14589144
    • 14589148
    • 14589149
    • 14589151
    • 14589154
    • 14589159
Amount recalled
35,596 devices in total

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

Symbiq Infusers have the potential to experience a white screen during titration of a Keep Vein Open (KVO) delivery. This can allow the clinician to select the "NEXT" button prior to completion of the programming. If this error occurs, a delay in therapy could occur and potentially result in significant injury.

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 Dec 15, 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.