Reported Jul 6, 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
145890031458900814589009145890121458901314589014145890151458901714589020145890221458902814589030145890311458903314589034145890351458904314589046145890481458904914589050145890531458905714589060145890631458906414589066145890681458907214589078145890821458908314589086145890921458909514589100145891011458910514589108145891101458911114589116145891171458911814589121145891271458913114589133145891351458913614589137145891391458914014589141145891441458914814589149145891511458915414589159
- Amount recalled
- 15,285
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
- Nationwide
Why it was recalled
Frequent Proximal Occlusion Alarms (POAs) occurring on Symbiq devices with list numbers 16026 and 16027. When there are false alarms, the pump will continue to alarm even though there is no occlusion present. False POAs could result in a delay/interruption in therapy, and require the clinician to reset the alarm multiple times or to replace the pump.
This product could cause temporary or reversible health problems — stop using it.
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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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