Additional information regarding this adverse event was received on 19 november 2021 and the investigation was concluded on 15 december 2021.The patient suffered a fall due to an unknown reason which caused soft tissue damage.The surgeon performed a soft tissue repair during the surgery and did not revise any of the eleos implants.The device was not returned for evaluation.The root cause of the patient's fall could not be determined.The device history records and sterilization batch records were reviewed and no issues during manufacturing or sterilization were identified that could have contributed to this complaint.If any additional information is obtained, a supplemental mdr will be filed accordingly.Multiple mdr reports were submitted for this event: #3013450937-2021-00234, #3013450937-2021-00235, #3013450937-2021-00236, #3013450937-2021-00321, #3013450937-2021-00322, #3013450937-2021-00324, #3013450937-2021-00325, #3013450937-2021-00326, #3013450937-2021-00327.
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