It was reported that there was an issue with collect.No.Qas knee implants vega as a result of having the product implanted, the patient has experienced left knee pain, limited mobility, and difficulty walking.The primary surgery occurred in 2016, and there was no reported revision surgery.All available information has been provided at this time, if additional information becomes available the complaint will be updated accordingly.The adverse event / malfunction is filed under xc reference (b)(4).
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