MAUDE Adverse Event Report: ETHICON INC. PROLENE MESH 3INX6IN; MESH, SURGICAL, POLYMERIC

Catalog Number	PMII
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Abdominal Pain (1685); Adhesion(s) (1695); Hernia (2240); Obstruction/Occlusion (2422)
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported by an attorney that the patient underwent incisional hernia repair on (b)(6) 2008 and mesh was implanted.It was reported that the patient underwent repair of recurrent incisional hernia on (b)(6) 2008 and mesh was implanted during which the surgeon noted multiple adhesions between the previous mesh and the bowel and omentum.It was reported that the patient underwent repair of recurrent incisional hernia, excision of mesh and lysis of adhesions on (b)(6) 2010 and mesh was implanted.It was reported that the patient underwent multiple recurrent incisional hernia repairs with wound infection on (b)(6) 2010.It was reported that the patient underwent exploration of midline surgical wound pulsed irrigation and placement of vac device on (b)(6) 2010.It was reported that the patient underwent debridement of abdominal wound and wound vac placement on (b)(6) 2010 during which the surgeon noted midline scar had a granulating area of the wound was excluded from the surgical field, there was nonhealing abdominal wound and abscess cavity was encountered.It was reported that the patient experienced chronic abdominal pain, and intermittent bowel obstruction.Other procedure was captured in a separate file.No additional information can be provided.
Additional Manufacturer Narrative
Date sent to the fda: 10/31/2024 d4: udi: as the lot number for the device involved in the event was for dhr review, the full udi is currently not available.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.(b)(4) submitted for adverse event which occurred on (b)(6)2008.(b)(4) submitted for adverse event which occurred on (b)(6)2010.(b)(4) submitted for adverse event which occurred on (b)(6)2010.(b)(4) submitted for adverse event which occurred on (b)(6)2010.(b)(4) submitted for adverse event which occurred on (b)(6)2010.This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information prior to the required reporting date.This report does not reflect a conclusion by ethicon, or its employees that the report constitutes an admission that the product, ethicon, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.
Additional Manufacturer Narrative
Date sent to the fda: 11/14/2024.Additional information: d4 (expiration), h4.Corrected information: d4 (primary udi #).A review of the batch manufacturing records was conducted and the batch met all finished goods release criteria.This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information prior to the required reporting date.This report does not reflect a conclusion by ethicon, or its employees that the report constitutes an admission that the product, ethicon, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.

• Brand Name: PROLENE MESH 3INX6IN
• Common Device Name: MESH, SURGICAL, POLYMERIC
• Manufacturer (Section D): ETHICON INC.; 1000 route 202; raritan NJ 08869
• Manufacturer (Section G): ETHICON INC.-SAN LORENZO PR; road 183, km 8.3; san lorenzo PR 00754
• Manufacturer Contact: elba bello ; 1000 route 202; raritan, NJ 08869 ; 9083863534
• MDR Report Key: 20584829
• Report Number: 2210968-2024-11337
• Device Sequence Number: 8714372
• Product Code: FTL
• UDI-Device Identifier: 10705031049024
• UDI-Public: (01)10705031049024(17)130131(10)AER413
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K180829
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2008
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 10/31/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 01/31/2013
• Device Catalogue Number: PMII
• Device Lot Number: AER413
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 10/23/2024
• Supplement Date Received by Manufacturer: 11/05/2024
• Initial Report FDA Received Date: 10/31/2024
• Supplement Report FDA Received Date: 11/14/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 05/28/2008
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Female