Catalog Number PHY1520V |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Abdominal Pain (1685); Adhesion(s) (1695); Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)
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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 hernia repair surgery on (b)(6) 2014 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 the fda: 3/28/2022.Additional b5 narrative: it was reported that the patient underwent hernia repair surgery on (b)(6) 2014 and mesh was implanted.
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Manufacturer Narrative
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Date sent to the fda: 4/4/2022 additional information: a1, a2, b7, d1, d2a, d4 additional b5 narrative: it was reported that the patient experienced abdominal pain and adhesions following surgery.(b)(4) submitted for adverse event which occurred on (b)(6) 2014.(b)(4) submitted for adverse event which occurred on (b)(6) 2018.
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Manufacturer Narrative
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Date sent to the fda: 4/12/2022.A review of the batch manufacturing records was conducted and the batch met all finished goods release criteria.
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Search Alerts/Recalls
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