The account returned 1 ethmsm20 stating that, "clips did not fire correctly" and that during the procedure the vessel was severed.The device was examined and subjected to full visual and functional testing.Outside of the presence of contaminants consistent with patient contact and use in the field, the device passed its visual inspection.The jaws were in alignment and the clip retainer was in position.The functionality of the device was tested via firing the device.The device was shipped to the field with 17 clips for use as noted by the number written in ink on the handle.The device was returned with 8 clips remaining.The device fired all 8 remaining clips, producing clips off appropriate pinch and alignment without interruption until all clips were spent.No defect was displayed by the device, nor were any of the clips found to displaying any features that would result in an injury.Based on this evidence the account's complaint could not be duplicated nor confirmed.A device history record review was performed, and no discrepancies were noted.Manufacturer's ref.No: (b)(4).
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