MAUDE Adverse Event Report: DAVOL INC., SUB. C.R. BARD, INC. -1213643 3DMAX; SURGICAL MESH

Catalog Number	0115320
Medical Device Problem Code	Migration (4003)
Health Effect - Clinical Codes	Pain (1994); Hernia (2240)
Date of Event	03/05/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
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-nov-2009) is considered to be a best estimate.This emdr represents the 3dmax mesh (device 2).An additional supplemental emdr was submitted to represent the 3dmax 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.
Event or Problem Description
Per information provided: on (b)(6) 2010 - patient was diagnosed with bilateral hernia thereby underwent laparoscopic repair with implant of 3dmax mesh (device 1 - left and device 2 - right).Per operative notes, "a small incision was made in the lower abdomen in the left inguinal region.The left inguinal hernia sac was dissected out.A 3dmax mesh (device 1) was placed into the left inguinal floor and secured it with sutures.Another incision was made into the right inguinal floor.The hernia sac was dissected out.A 3dmax mesh (device 2) was placed into the right inguinal floor and secured it with sutures." on (b)(6) 2019 - patient was diagnosed with bilateral reducible recurrent inguinal hernias, pain, thereby underwent laparoscopic repair of a left recurrent direct inguinal hernia with implant of unknown mesh and repair of a right recurrent direct inguinal hernia using existing old mesh (device 2).Per operative notes, "an incision was made into the left inguinal region.The hernia sac was dissected out.An unknown mesh was placed into the left inguinal region and secured it with sutures.Another incision was made into the right inguinal floor.The hernia sac was dissected out.The old mesh had become dislodged from its attachments.The old mesh (device 2) was attached again with sutures again with good coverage primarily.".

• Brand Name: 3DMAX
• 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: 25653294
• Report Number: 1213643-2026-00806
• Device Sequence Number: 13198914
• Product Code: FTL
• UDI-Device Identifier: 00801741030758
• UDI-Public: (01)00801741030758(17)141128(10)HUTK0895
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K081010
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2010
• Reporter Type: Manufacturer
• Report Source: Other,Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 06/17/2026

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: 11/28/2014
• Device Catalogue Number: 0115320
• Device Lot Number: HUTK0895
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/11/2026
• Initial Report FDA Received Date: 06/29/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 11/15/2009
• 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 Age: 52 YR
• Patient Sex: Male