Model Number PHSM |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
|
Patient Problems
Abdominal Pain (1685); Hematoma (1884); Unspecified Infection (1930); Pain (1994); Hernia (2240); Deformity/ Disfigurement (2360); Cramp(s) /Muscle Spasm(s) (4521); Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)
|
Event Type
Injury
|
Event Description
|
It was reported by an attorney that the patient underwent hernia repair surgery on (b)(6) 2007 and mesh was implanted.It was reported that the patient underwent removal surgery and recurrent hernia repair surgery on (b)(6) 2020.It was reported that the patient experienced severe pain, infection, hematoma, muscle spasms, stabbing abdominal pain, abdominal disfigurement and fluid buildup.No additional information was provided.
|
|
Manufacturer Narrative
|
(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.
|
|
Manufacturer Narrative
|
(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.
|
|
Event Description
|
It was reported by an attorney that the patient underwent hernia repair surgery on (b)(6) 2007 and mesh was implanted.It was reported that the patient underwent removal surgery and recurrent hernia repair surgery on (b)(6) 2020.It was reported that the patient experienced severe pain, infection, hematoma, muscle spasms, stabbing abdominal pain, abdominal disfigurement and fluid buildup.No additional information was provided.
|
|
Manufacturer Narrative
|
Date sent to the fda: 2/28/2022.A review of the batch manufacturing records was conducted and the batch met all finished goods release criteria.
|
|
Manufacturer Narrative
|
Date sent to the fda: 06/30/2022.
|
|
Search Alerts/Recalls
|