The device was returned to the factory for evaluation.It showed no signs of clinical usage.There was evidence of blood.The delivery device was returned outside the loading device.The tension spring assembly, anchor tab, and seal were returned outside the devices.The green slide lock and the white plunger were not depressed on the delivery device.Based upon the eval results, the reported complaint was confirmed for failure to load.A lot history record review was completed for the reported product lot number.There was no nonconformance recorded in the lot history.Internal corrective action (wy-2013-35) issued for this failure mode.(b)(4).
|