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.
FDA MedWatch Safety Alert. Symbios GOPump Elastomeric Infusion PumpKit: Class 1 Recall. March 18, 2013.