MAUDE Adverse Event Report: DAVOL INC., SUB. C.R. BARD, INC. -1213643 VENTRALEX ST; SURGICAL MESH

Catalog Number	5950009
Medical Device Problem Code	Patient-Device Incompatibility (2682)
Health Effect - Clinical Codes	Unspecified Infection (1930); Hernia (2240); Obstruction/Occlusion (2422)
Date of Event	08/14/2023
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
No conclusions can be made.The patient's attorney alleges adverse patient outcome associated with the hernia mesh used to treat the patient, including disability, infection, hernia recurrence, obstruction and device explant.The instructions-for-use supplied with the device list infection and hernia recurrence as possible complications.A review of the manufacturing records was performed and found the lot was manufactured to specification.Should additional information be provided, a supplemental emdr will be submitted.Note: section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.
Event or Problem Description
Attorney alleges that the patient underwent incisional hernia repair surgery with implant of ventralex st on (b)(6) 2015.It was alleged that the patient had ventral hernia repair thereby underwent additional surgical intervention for small bowel resection and mesh removal on (b)(6) 2023.As per the operative report ¿indicate that the small bowel was resected off the mesh and the open portion was resected using a jia stapler.The small bowel was then re-anastomosed using a 55mm selectable linear cutter with staples and a 60mm ta stapler with dst series.The mesh was then resected using blunt dissection with metzenbaum scissors.¿ attorney alleges that the patient experiencing infections, recurrence, chronic pain which have impaired daily activities.Attorney alleges general allegations for "past, present, and future damages, including but not limited to, mental and physical pain and suffering for severe and permanent personal injuries sustained by the patient." it is also alleged that the device was defective.
Additional Manufacturer Narrative
No conclusions can be made.The patient's attorney alleges adverse patient outcome associated with the hernia mesh used to treat the patient, including disability, infection, hernia recurrence, obstruction and device explant.The instructions-for-use supplied with the device list infection and hernia recurrence as possible complications.A review of the manufacturing records was performed and found the lot was manufactured to specification.Addendum: h11: this supplemental emdr is submitted to correct the annex b code and term.Note, the manufacturing date (15-nov-2013) is considered to be a best estimate.Note: section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.
Event or Problem Description
Attorney alleges that the patient underwent incisional hernia repair surgery with implant of ventralex st on (b)(6) 2015.It was alleged that the patient had ventral hernia repair thereby underwent additional surgical intervention for small bowel resection and mesh removal on (b)(6) 2023.As per the operative report ¿indicate that the small bowel was resected off the mesh and the open portion was resected using a jia stapler.The small bowel was then re-anastomosed using a 55mm selectable linear cutter with staples and a 60mm ta stapler with dst series.The mesh was then resected using blunt dissection with metzenbaum scissors.¿ attorney alleges that the patient experiencing infections, recurrence, chronic pain which have impaired daily activities.Attorney alleges general allegations for "past, present, and future damages, including but not limited to, mental and physical pain and suffering for severe and permanent personal injuries sustained by the patient." it is also alleged that the device was defective.

• Brand Name: VENTRALEX ST
• Common Device Name: SURGICAL MESH
• Manufacturer (Section D): DAVOL INC., SUB. C.R. BARD, INC. -1213643; 100 crossings blvd.; warwick RI 02886
• Manufacturer (Section G): BARD SHANNON LIMITED -3005636544; san geronimo industrial park; lot #1, road #3, km 79.7; humacao PR 00791
• Manufacturer Contact: andrew topoulos ; 100 crossings blvd.; warwick, RI 02886 ; 8005566756
• MDR Report Key: 22932355
• Report Number: 1213643-2025-00802
• Device Sequence Number: 10231423
• Product Code: FTL
• UDI-Device Identifier: 00801741031496
• UDI-Public: (01)00801741031496(17)151128(10)HUXK0039
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• PMA/510(K) Number: K101928
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2015
• Device Explanted Year: 2023
• Reporter Type: Manufacturer
• Report Source: Other,Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 09/11/2025

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 Expiration Date: 11/28/2015
• Device Catalogue Number: 5950009
• Device Lot Number: HUXK0039
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/18/2025
• Supplement Date Received by Manufacturer: 09/11/2025
• Initial Report FDA Received Date: 09/02/2025
• Supplement Report FDA Received Date: 09/18/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 11/15/2013
• 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: Disability; Required Intervention
• Patient Sex: Male