MAUDE Adverse Event Report: DAVOL INC., SUB. C.R. BARD, INC. -1213643 MESH ¿ COMPOSIX L/P; SURGICAL MESH

Catalog Number	0134790
Medical Device Problem Codes	Defective Device (2588); Patient-Device Incompatibility (2682); Patient Device Interaction Problem (4001)
Health Effect - Clinical Codes	Adhesion(s) (1695); Pain (1994); Hernia (2240); Insufficient Information (4580)
Date of Event	07/27/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
No conclusions can be made.The patient's attorney alleges "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"; however, no details have been provided.No lot number has been provided; therefore, a review of the manufacturing records is not possible.This emdr represents the bard/davol mesh ¿ composix l/p (device #2).An additional emdr was submitted to represent the bard/davol ventralex mesh (device #1).Should additional information be provided, a supplemental emdr will be submitted.Not returned.
Event or Problem Description
Attorney alleges that the patient underwent surgery for implant of unspecified bard/davol ventralex and composix lp on (b)(6) 2011 and/or (b)(6) 2013.As reported, the patient is making a claim for an adverse patient outcome against both devices.Attorney alleges that the patient sustained injuries on (b)(6) 2013 and (b)(6) 2020 due to the hernia mesh device.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 patient experienced emotional distress and the device was defective.
Additional Manufacturer Narrative
No conclusions can be made.The patient's attorney alleges "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"; however, no details have been provided.No lot number has been provided; therefore, a review of the manufacturing records is not possible.Addendum: this supplemental emdr is submitted to document additional information provided.Root cause is inconclusive, no conclusion can be made as to the extent to which the implant may have caused or contributed to the patient's postoperative course.Note, the manufacturing date (15-sep-2012) is considered to be a best estimate.Updated fields: a2, b2, b3, b4, b5, b7, d3, d4, d6a, d6b, g3, g6, h2, h4, h6, h10.This supplemental emdr represents the bard/davol mesh ¿ composix l/p (device 2).An additional supplemental emdr was submitted to represent the bard/davol ventralex mesh (device 1).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.H3 other text: not returned.
Event or Problem Description
Attorney alleges that the patient underwent surgery for implant of unspecified bard/davol ventralex and composix lp on (b)(6) 2011 and/or (b)(6) 2013.As reported, the patient is making a claim for an adverse patient outcome against both devices.Attorney alleges that the patient sustained injuries on (b)(6) 2013 and (b)(6) 2020 due to the hernia mesh device.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 patient experienced emotional distress and the device was defective.Addendum per additional information provided: (b)(6) 2011 ¿ patient was diagnosed with incisional hernia thereby underwent open repair with the implant of ventralex patch (device #1).Per operative notes, ¿a ventralex patch (device #1) was placed into fascial defects using sutures.¿ (b)(6) 2013 ¿ patient was diagnosed with recurrent incarcerated ventral incisional hernia thereby underwent open repair with the removal of mesh.Per operative notes, ¿adhesion between small bowel and mesh were lysed.The mesh (device #1) was completely excised.A composix l/p mesh (device #2) was placed and sewn to defect.¿ (b)(6) 2020 ¿ patient was diagnosed with recurrent incarcerated incisional hernia thereby underwent open repair with the removal of mesh (device #2).Per operative notes, ¿at cranial edge of hernia defect, there were densely adhered small bowel to previously placed mesh (device #2).A well incorporated mesh (device #2) was removed, and synthetic mesh was placed to reconstruct the sac using sutures.¿.

• Brand Name: MESH ¿ COMPOSIX L/P
• 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 ; 4018258495
• MDR Report Key: 14841074
• Report Number: 1213643-2022-95000
• Device Sequence Number: 19420978
• Product Code: FTL
• UDI-Device Identifier: 00801741031304
• UDI-Public: (01)00801741031304(17)171028(10)HUWI1345
• Combination Product (Y/N): N
• Initial Reporter State: RI
• Initial Reporter Country: US
• PMA/510(K) Number: K061754
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2013
• Device Explanted Year: 2020
• 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: 10/28/2017
• Device Catalogue Number: 0134790
• Device Lot Number: HUWI1345
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 06/23/2022
• Supplement Date Received by Manufacturer: 08/21/2025
• Initial Report FDA Received Date: 06/28/2022
• Supplement Report FDA Received Date: 09/11/2025
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 09/15/2012
• 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; Disability
• Patient Age: 55 YR
• Patient Sex: Female