Catalog Number PHY2025V |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Adhesion(s) (1695); Pain (1994); Hernia (2240); Injury (2348)
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Event Type
Injury
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Manufacturer Narrative
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(b)(4).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.
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Event Description
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It was reported by an attorney that the patient underwent a hernia repair procedure on (b)(6) 2015 and mesh was implanted.It was reported the patient experienced an undisclosed adverse event.No additional information was provided.
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Manufacturer Narrative
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Date sent to fda: 2/18/2019.Additional narrative: it was reported that the patient experienced pain, adhesion and recurrent hernia.It was reported the patient underwent mesh removal on (b)(6) 2018.
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Manufacturer Narrative
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Date sent to the fda: 04/22/2020.Corrected information: manufacturing site name.
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Search Alerts/Recalls
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