Model Number PVPM |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Unspecified Infection (1930); Pain (1994); Hernia (2240); Not Applicable (3189)
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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) 2013 and mesh was implanted.It was reported that the patient underwent removal surgery on (b)(6) 2014.It was reported that the patient experienced severe and chronic pain.No additional information was provided.
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Manufacturer Narrative
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Date sent to the fda: 10/25/2021.A review of the batch manufacturing records was conducted and the batch met all finished goods release criteria.
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Manufacturer Narrative
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Date sent to the fda: 10/13/2021 additional information: a2, b7, d3 additional b5 narrative: it was reported that the patient experienced recurrent incisional hernia and infection following surgery.
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Search Alerts/Recalls
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