The FDA publish details on the Symbios GOPump Elastomeric Infusion PumpKit: Class 1 Recall

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Intravenous products: The FDA report on the Symbios GOPump Elastomeric Infusion PumpKit: Class 1 Recall “Symbios Medical Products, LLC sent its customers an “URGENT MEDICAL DEVICE RECALL” notification letter detailing the reason for recall and products listed. The reason for the recall is that 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. Refer to the Recall Notice for a list of kit part numbers.”

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