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

Catalog Number	0115321
Medical Device Problem Code	Patient-Device Incompatibility (2682)
Health Effect - Clinical Codes	Adhesion(s) (1695); Hernia (2240)
Date of Event	01/07/2020
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-jul-2017) 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) 2017 - patient was diagnosed with bilateral pantaloons hernia thereby underwent laparoscopic repair with implant of 3dmax mesh (device 1 and 2).Per op notes, "the left then the right lower quadrants peritoneum were divided.Adhesions from incarcerated left/sigmoid colon was noted.A 3dmax mesh (device 1) was placed on the left groin and secured to the fascia with sutures.A 3dmax mesh (device 2) was placed on the right groin and secured to the fascia with sutures.All three defects the direct, indirect and femoral defects were covered." on (b)(6) 2020 - patient was diagnosed with bilateral recurrent inguinal hernias and adhesions between both old meshes and cords thereby underwent robotic laparoscopic assisted repair with implant of 3dmax mesh (device 3 and 4).Per op notes, "the left then the right lower quadrants peritoneum were divided.Adhesions from previous bilateral inguinal herniorrhaphy was noted.Extensive lysis of adhesions between the old meshes (device 1 and 2) and the cords bilaterally was performed.A 3dmax mesh (device 3) was placed on the left groin and secured to the fascia with sutures.A 3dmax mesh (device 4) was placed on the right groin and secured to the fascia with sutures.All three defects the direct, indirect and femoral defects were covered.".

• 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: 25241474
• Report Number: 1213643-2026-00665
• Device Sequence Number: 18778596
• Product Code: FTL
• UDI-Device Identifier: 00801741030765
• UDI-Public: (01)00801741030765(17)220728(10)HUBU1189
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: K081010
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: Other,Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 05/19/2026

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: 07/28/2022
• Device Catalogue Number: 0115321
• Device Lot Number: HUBU1189
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/11/2026
• Initial Report FDA Received Date: 05/21/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 07/15/2017
• 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: 60 YR
• Patient Sex: Male
• Patient Weight: 85 KG