ClearanceBrief
Recall Z-0069-2013 ยท FRN Pump, Infusion

Hospira Inc.

Symbiq One 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 16026-01 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

DateOct 19, 2012 (initiated Aug 29, 2012)
StatusTerminated
ReasonThe 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.
Root causeDevice Design
ActionHospira sent an Urgent Device Correction letter dated August 29, 2012, to all affected customers. Customers have been informed of reports that 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. The users were instruct
Quantity19,614 units
DistributionWorldwide Distribution - USA (nationwide) Puerto Rico and Internationally to Canada
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K041550HOSPIRA PHOENIX INFUSION SYSTEM WITH HOSPIRA MEDNET SOFTWARE
Abbott Laboratories, Jun 30, 2004
K110901SYMBIQ INFUSION AND ADMINSTRATION SET
Hospira, Inc., Mar 5, 2012