It was reported by an attorney that the patient underwent hernia repair surgery on (b)(6) 2016 and mesh was implanted.It was reported that the patient underwent removal surgery on (b)(6) 2017 during which the surgeon noted he resected the sac and portion of the old mesh.It was reported that the patient underwent recurrent hernia repair surgery on (b)(6) 2020.It was reported that the patient underwent recurrent hernia repair surgery on (b)(6) 2021.It was reported that the patient experienced severe pain, nausea, diarrhea, chills, inflammation, loss of appetite and extreme weight loss.No additional information was provided.
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Date sent to the fda: 10/25/2022.To date, the device has not been returned.If the product is returned for evaluation, any further information derived from the evaluation will be submitted in a supplemental 3500a form.(b)(4) submitted for adverse event which occurred on (b)(6) 2017.(b)(4) submitted for adverse event which occurred on (b)(6) 2020.(b)(4) submitted for adverse event which occurred on (b)(6) 2021.
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