Skip to content
Recall Observatory FDA recall evidence

Device product

Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Hospira, Inc., Lake Forest, IL 60045 USA, Made in Costa Rica; List Number 16027-01 Device is a general purpose infusion pump designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes, blood and blood products for parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural

Z-0070-2013

August 29, 2012

Class I

Product summary

Firm
Hospira Inc.
Event
Event 63056
Status
Terminated
Classification
Class I
Quantity
14,067 units
Official record key
device-enforcement:Z-0070-2013

Official wording

Reason: The Symbiq pump touchscreen may not respond to user selection, may experience a delayed response, or may register a different value from the value selected by the user. Failure of the touchscreen to respond to user input could result in a delay in therapy or result in over delivery or under delivery of medication if the user does not confirm the programmed values on the pump's confirmation screen prior to starting the infusion.

Code information: List Number 16027-01, all serial numbers

Distribution pattern: Worldwide Distribution - USA (nationwide) Puerto Rico and Internationally to Canada

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The Symbiq pump touchscreen may not respond to user selection, may experience a delayed response, or may register a different value from the value selected by the user. Failure of the touchscreen to respond to user input could result in a delay in therapy or result in over delivery or under delivery of medication if the user does not confirm the programmed values on the pump's confirmation screen prior to starting the infusion.