Reported Nov 2, 2016 · Terminated

Symbiq One 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 One 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

    • 14339017
    • 14339062
    • 14339063
    • 14339066
    • 14339071
    • 14339072
    • 14339076
    • 14339078
    • 14339079
    • 14339084
    • 14339086
    • 14339087
    • 14339089
    • 14339090
    • 14339091
    • 14339095
    • 14339097
    • 14339098
    • 14339099
    • 14339102
    • 14339104
    • 14339105
    • 14339107
    • 14339108
    • 14339111
    • 14339113
    • 14339114
    • 14339115
    • 14339116
    • 14339119
    • 14339121
    • 14339125
    • 14339128
    • 14339130
    • 14339133
    • 14339136
    • 14339138
    • 14339139
    • 14339140
    • 14339141
    • 14339142
    • 14339145
    • 14339146
    • 14339149
    • 14339150
    • 14339152
    • 14339154
    • 14339155
    • 14339158
    • 14339168
    • 14339171
    • 14339172
    • 14339179
    • 14339180
    • 14339185
    • 14339190
    • 14339192
    • 14339194
    • 14339195
    • 14339200
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, 6:15 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.