Symbios GOPump Elastomeric Infusion PumpKit: Class I Recall
MedSun: Newsletter #83, April 2013

FDA MedWatch Safety Alert

The flow restrictor bead may become displaced from its' fitting which may permit solutions to flow at a higher rate than intended. This product may cause serious adverse health consequences, including death. These kits were distributed between Sept. 10, 2012 and Feb. 11, 2013.

Additional Information:

FDA MedWatch Safety Alert. Symbios GOPump Elastomeric Infusion PumpKit: Class 1 Recall. March 18, 2013.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm344352.htm


MedSun Newsletters are available at www.fda.gov/cdrh/medsun