A visual assessment of the returned complaint inserter/compressor showed an instrument with minimal use, as identified by crisp laser markings and a lack of surface scratches.The pin of the instrument distal tip was fractured where it connects with the instrument handle.A functionality assessment was not performed due to the damaged condition of the returned inserter/compressor, which was removed from distributable inventory.It may be possible that application of excessive compression force may have contributed to one of the instrument distal tips fracturing from the instrument.The instrument tip is secured into the instrument handle with a cylinder that has minor movement to allow for implant engagement and patient anatomy.It may be possible that plate angulation due to patient anatomy or over compressing the instrument may concentrate applied force to the instrument distal tip, resulting in an instrument malfunction.
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