ETHICON INC. TENSION FREE VAGINAL TAPE UNKNOWN PRODUCT; MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC
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Device Problem
Migration (4003)
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Patient Problems
Micturition Urgency (1871); Incontinence (1928); Pain (1994); Urinary Tract Infection (2120); Urinary Frequency (2275)
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Event Type
Injury
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Manufacturer Narrative
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Date sent to the fda: 9/15/2023.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.This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information prior to the required reporting date.This report does not reflect a conclusion by ethicon, or its employees that the report constitutes an admission that the product, ethicon, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.
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Event Description
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It was reported by an attorney that the patient underwent a gynecological surgical procedure on (b)(6) 2007 and mesh was implanted.It was reported that the patient experienced back pain, stress incontinence, urgency, urge incontinence, nocturia, frequency, thrush, hip pain, pelvic pain and urinary tract infections.No additional information was provided.
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Manufacturer Narrative
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Product complaint # (b)(4).Investigation summary : product was not returned.Based on the information available, no further action is required at this time.Complaint information is trended on a regular basis to determine if further investigation is warranted.If additional information is made available, the investigation will be updated as applicable.
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Search Alerts/Recalls
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