MAUDE Adverse Event Report: SOFRADIM PRODUCTION SAS PROGRIP; MESH, SURGICAL, POLYMERIC

Model Number LPG1510

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Abscess (1690); Hematoma (1884); Ischemia (1942); Scar Tissue (2060); Hernia (2240); Unspecified Tissue Injury (4559)

Event Type  Injury  

Manufacturer Narrative

Concomitant medical product: (lot # prg0353x).If information is provided in the future, a supplemental report will be issued.

Event Description

The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of bilateral inguinal hernias by laparoscopic repair and an umbilical hernia.It was reported that after the implant, the patient experienced hematoma, ischemia, clotted blood, scarring, abscess, recurrence, scar tissue, fascia attenuation, and spermatic cord involvement.Post-operative patient treatment included dissection of old mesh, mesh resuture to the inguinal floor, incision/drainage of hematoma, orchiectomy, hernia repair with new mesh, hernia repair with old mesh, chunks of clotted blood removed, j-prat drain placed, dissection of scar tissue, left ischemic testicle amputation, and spermatic cord resection.

• Brand Name: PROGRIP
• Type of Device: MESH, SURGICAL, POLYMERIC
• Manufacturer (Section D): SOFRADIM PRODUCTION SAS; 116 avenue du formans; trevoux 01600 ; FR 01600
• Manufacturer (Section G): SOFRADIM PRODUCTION SAS; 116 avenue du formans; trevoux 01600 ; FR 01600
• Manufacturer Contact: tracy landers ; 5920 longbow drive; boulder, CO 80301 ; 3035816943
• MDR Report Key: 11867267
• MDR Text Key: 252173268
• Report Number: 9615742-2021-01377
• Device Sequence Number: 1
• Product Code: FTL
• UDI-Device Identifier: 10884521513136
• UDI-Public: 10884521513136
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K120897
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: consumer
• Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date: 05/21/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 05/21/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Expiration Date: 06/30/2020
• Device Model Number: LPG1510
• Device Catalogue Number: LPG1510
• Device Lot Number: PRG0988X
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 05/05/2021
• Date Device Manufactured: 07/28/2017
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Weight: 93