It was reported that a patient received a total shoulder implant on (b)(6) 2018.The patient was revised on (b)(6) 2018 after an infection was diagnosed at the 4-week postop visit.The patient was stable leaving the operating room.The devices were kept by the hospital and sent to pathology.This is one of ten products involved with the reported event and the associated manufacturer report numbers are 1038671-2018-00366, 1038671-2018-00367, 1038671-2018-00368, 1038671-2018-00369, 1038671-2018-00370, 1038671-2018-00371, 1038671-2018-00372, 1038671-2018-00373, 1038671-2018-00374 and 1038671-2018-00375.
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