Model Number PCDN1 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Adhesion(s) (1695); Foreign Body Reaction (1868); Inflammation (1932); Pain (1994); Hernia (2240); Discomfort (2330)
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Event Type
Injury
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Manufacturer Narrative
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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) 2010 and mesh was implanted.It was reported that the patient underwent revision surgery on (b)(6) 2017.It was reported that the patient experienced severe and chronic pain/discomfort, inflammation, extensive abdominal wall adhesions and foreign body giant cell reaction.No additional information was provided.
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Manufacturer Narrative
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Date sent to the fda: 6/22/2022.Additional b5 narrative: it was reported that the patient experienced hernia recurrence.
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Manufacturer Narrative
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Date sent to the fda: 7/18/2022 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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