MAUDE Adverse Event Report: ETHICON INC. ULTRAPRO* PART. ABSORB. MESH; MESH, SURGICAL, POLYMERIC

Catalog Number	UMR3
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Adhesion(s) (1695); Pain (1994)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Date sent to the fda: 8/01/2025.D4: udi: as the lot number for the device involved in the event was not provided, 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.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.
Event or Problem Description
It was reported by an attorney that patient underwent revision surgery on (b)(6) 2010 and a mesh was implanted.It was previously reported that the patient had hernia repair surgery on (b)(6) 2009 and two (2) mesh were implanted.It was also previously reported that the patient underwent revision surgery on (b)(6) 2010 and a mesh was implanted.It was reported that the patient experienced adhesion and pain.Other procedure was captured on a separate file.No additional information was provided.
Additional Manufacturer Narrative
Date sent to the fda: 8/3/2025.Corrected information: b5, b7.Additional b5 narrative: it was reported that patient underwent revision surgery on (b)(6) 2010 and ultrapro was implanted.It was previously reported that the patient had hernia repair surgery on (b)(6) 2009 and two (2) proceed were implanted.It was also previously reported that the patient underwent revision surgery on (b)(6) 2010 and ultrapro was implanted.It was reported that the patient experienced adhesion and pain.Other procedure was captured on a separate file.No additional information was provided.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.

• Common Device Name: MESH, SURGICAL, POLYMERIC
• Manufacturer (Section D): ETHICON INC.; 1000 route 202; raritan NJ 08869
• Manufacturer (Section G): ETHICON INC.; 1000 route 202; raritan 08869 0151
• Manufacturer Contact: elba bello ; 1000 route 202; raritan, NJ 08869 ; 9083863534
• MDR Report Key: 22687028
• Report Number: 2210968-2025-08916
• Device Sequence Number: 21194157
• Product Code: FTL
• UDI-Device Identifier: 10705031132498
• UDI-Public: (01)10705031132498
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K033337
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2010
• 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): 08/01/2025

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 Catalogue Number: UMR3
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 07/22/2025
• Supplement Date Received by Manufacturer: 08/01/2025
• Initial Report FDA Received Date: 08/01/2025
• Supplement Report FDA Received Date: 08/03/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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