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
145890031458900814589009145890121458901314589014145890151458901714589020145890221458902814589030145890311458903314589034145890351458904314589046145890481458904914589050145890531458905714589060145890631458906414589066145890681458907214589078145890821458908314589086145890921458909514589100145891011458910514589108145891101458911114589116145891171458911814589121145891271458913114589133145891351458913614589137145891391458914014589141145891441458914814589149145891511458915414589159
- 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.
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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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