This follow-up report is submitted to fda in accord with applicable regulations- and as indicated by terumo cardiovascular systems in the initial report submitted to the fda on 05/06/2015.The actual device was visually inspected upon receipt revealing breakage and cracking in the reservoir lid.The damage, located in the area around the venous port, is consistent with an applied external force as this is the most external point in the package unit.Since the product is 100% visually inspected and leak tested during the manufacturing process, the reported damage is most likely due to excessive force post manufacturing; however the cause of the device is unknown.A review of the device history record revealed there were no production related anomalies.All available information has been placed on file in quality management for appropriate tracking, trending and follow-up.
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