PROLENE PHSMRecalls & reported problems

Summary

The FDA's MAUDE database contains 360 adverse event reports that list this exact device (DI 10705031048997), received between Mar 22, 2018 and Aug 31, 2026 — classified as 353 injuries, 7 malfunctions.

The most frequently reported specific device problem is “Migration” (12 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 360 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 31, 2026Device Markings/Labelling Problem

  It was reported that during an inventory tracking process on an unknown date, an error occurred while scanning the UDI of the mesh product. The UDI's expiration date is (b)(6) 2025, whereas the expiration date printed on the packaging is (b)(6) 2027. There was no patient involvement and no adverse patient consequences.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50524346 ↗
• InjuryJun 11, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN INGUINAL HERNIA REPAIR PROCEDURE ON (B)(6) 2008 AND MESH WAS IMPLANTED. THE PATIENT REPORTED THEY HAD: CHRONICALLY SHARP PAIN IN THE RIGHT GROIN. OBSTRUCTION OF THE RIGHT SEMINAL FLUID, INFLAMMATION OF THE PROSTATE, EPIDIDYMIS AND TESTICLE OF THE RIGHT AND RIGHT SEMINAL VESICLES. CHRONIC PAIN OF THE RIGHT TESTIS. REOPERATION MADE ON (B)(6) 2015. RELY ON REMOVING A PIECE OF SURGICAL MESH WITH SOLID INFILTRATION FROM THIS SEMINAL FLUID. MULTIPLE STEROID LOCKS, RIGHT GROIN INJECTION LIGNOCAINE. TREATED IN THE CLINIC OF PAIN TREATMENT WITH A PERMANENT EFFECT. THE NEED FOR MULTIPLE REHABILITATION TREATMENTS CARRIED OUT IN STATIONS AND SANATORIUMS. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: Erosion; Inflammation; Insufficient Information; Obstruction/Occlusion; Pain

  MAUDE report 25477127 ↗
• InjuryApr 17, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY THE PATIENT THAT THEY UNDERWENT AN INGUINAL HERNIA REPAIR PROCEDURE ON (B)(6) 2024 AND MESH WAS IMPLANTED. SINCE IMPLANTATION, THE PATIENT HAS EXPERIENCED A SEVERE AND DISABLING DETERIORATION OF OVERALL HEALTH. THESE SYMPTOMS APPEARED GRADUALLY AND INTERMITTENTLY AFTER THE OPERATION, BUT THEY ARE NOW CHRONIC. THEIR INTENSITY VARIES FROM DAY TO DAY AND CAN REACH EXTREMELY SEVERE EPISODES THAT COMPLETELY PREVENT ME FROM LEAVING THE HOUSE. THE PATIENT REPORTS: LOCAL AND MECHANICAL SYMPTOMS: I FEEL A CONSTANT DISCOMFORT AT THE IMPLANTATION SITE WITH A CARDBOARD-LIKE STIFFNESS OF THE OPERATED AREA. I HAVE BECOME UNABLE TO CARRY LOADS OR EXERT ANY FORCE. ANY PHYSICAL STRAIN TRIGGERS SHOOTING PAINS OR A CRAWLING/BUZZING SENSATION THAT RADIATES INTO BOTH OF MY LEGS. NEUROLOGICAL AND MOTOR SYMPTOMS: I SUFFER FROM DIFFUSE NEUROPATHIC PAIN THROUGHOUT MY BODY. MY MOTOR ABILITIES IN THE LOWER LIMBS ARE SEVERELY IMPAIRED. COGNITIVELY, I EXPERIENCE PERSISTENT BRAIN FOG, MEMORY LOSSES, AND SIGNIFICANT CONCENTRATION DIFFICULTIES. DIFFUSE PAIN AND SYSTEMIC INVOLVEMENT: I HAVE CHRONIC BONE PAIN LOCALIZED IN MY LEGS, PELVIS, AND ARMS, AS WELL AS DIFFUSE PAIN ELSEWHERE IN MY BODY. MY

  Patient problems: Diarrhea; Discomfort; Memory Loss/Impairment; Pain

  MAUDE report 24913251 ↗
• InjuryApr 17, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY THE PATIENT THAT THEY UNDERWENT AN INGUINAL HERNIA REPAIR PROCEDURE ON (B)(6) 2024 AND MESH WAS IMPLANTED. SINCE IMPLANTATION, THE PATIENT HAS EXPERIENCED A SEVERE AND DISABLING DETERIORATION OF OVERALL HEALTH. THESE SYMPTOMS APPEARED GRADUALLY AND INTERMITTENTLY AFTER THE OPERATION, BUT THEY ARE NOW CHRONIC. THEIR INTENSITY VARIES FROM DAY TO DAY AND CAN REACH EXTREMELY SEVERE EPISODES THAT COMPLETELY PREVENT ME FROM LEAVING THE HOUSE. THE PATIENT REPORTS: LOCAL AND MECHANICAL SYMPTOMS: I FEEL A CONSTANT DISCOMFORT AT THE IMPLANTATION SITE WITH A CARDBOARD-LIKE STIFFNESS OF THE OPERATED AREA. I HAVE BECOME UNABLE TO CARRY LOADS OR EXERT ANY FORCE. ANY PHYSICAL STRAIN TRIGGERS SHOOTING PAINS OR A CRAWLING/BUZZING SENSATION THAT RADIATES INTO BOTH OF MY LEGS. NEUROLOGICAL AND MOTOR SYMPTOMS: I SUFFER FROM DIFFUSE NEUROPATHIC PAIN THROUGHOUT MY BODY. MY MOTOR ABILITIES IN THE LOWER LIMBS ARE SEVERELY IMPAIRED. COGNITIVELY, I EXPERIENCE PERSISTENT BRAIN FOG, MEMORY LOSSES, AND SIGNIFICANT CONCENTRATION DIFFICULTIES. DIFFUSE PAIN AND SYSTEMIC INVOLVEMENT: I HAVE CHRONIC BONE PAIN LOCALIZED IN MY LEGS, PELVIS, AND ARMS, AS WELL AS DIFFUSE PAIN ELSEWHERE IN MY BODY. MY

  Patient problems: Diarrhea; Discomfort; Memory Loss/Impairment; Pain

  MAUDE report 24913247 ↗
• InjuryMar 16, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT A BILATERAL HERNIA REPAIRS ON (B)(6) 2006 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED INGUINAL BULGING ON BOTH SIDES. NO ADDITIONAL INFORMATION WAS REPORTED.

  Patient problems: Swelling/ Edema

  MAUDE report 24602544 ↗
• InjuryMar 3, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY A PATIENT THAT THEY UNDERWENT A SURGICAL PROCEDURE FOR AN INGUINAL HERNIA ON (B)(6) 2021 AND MESH WAS USED. FOLLOWING MESH PLACEMENT, THE PATIENT EXPERIENCED ILEO-INGUINAL PAIN. THE PATIENT EXPERIENCED CONSTANT GENE ON FULL BLADDER AND PAIN LIKE STABBING SENSATION OF HEAVINESS AT THE LEVEL OF THE LEFT TESTICLE. THE PATIENT HAD PAIN ON ERECTIONS. FOLLOW-UP AT THE PAIN CENTER WITH ABOUT 5 PATCHES OF QUITENZA, THE LAST BEING IN (B)(6) 2025. THE PAIN WAS PARTLY CONTROLLED, BUT FOR 1 MONTH, THE SYMPTOMS HAVE RETURNED WITH AN INTENSITY OF 4 PLUS. CURRENT STATE OF THE PATIENT WAS REPORTED AS CONSTANT GENE, PAIN WITH EVA A 7 NEED FOR ANALGESIC AND A VELSATIS PATCH IF SEVERE PAIN. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: Pain

  MAUDE report 24502187 ↗
• InjuryFeb 6, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN RIGHT INGUINAL HERNIA REPAIR ON AN UNKNOWN DATE AND MESH WAS IMPLANTED. THE PATIENT DEVELOPED SEVERE AND DISABLING PAIN, DIAGNOSIS OF NEUROPATHIC PAIN WITH NO EFFECT OF USUAL PAINKILLERS TREATMENT WITH GABAPENTIN 600, 3 TAKEN DAILY. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Neuropathy; Pain

  MAUDE report 24283723 ↗
• InjuryFeb 6, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT A FEMORAL HERNIA REPAIR PROCEDURE (B)(6) 2014. POSTOPERATIVE COURSE WAS UNCOMPLICATED. THE PATIENT WAS DISCHARGED THE DAY AFTER SURGERY WITH MEDICATIONS. THE PATIENT DEVELOPED A RECURRENT LEFT INGUINAL HERNIA THAT WAS CONFIRMED ON ULTRASOUND AND UNDERWENT A REPAIR ON (B)(6) 2015. CURRENT PATIENT STATUS: SEVERE PAIN IN THE LEFT INGUINAL AREA (TWO HERNIA MESHES OVERLAPPING). THE PAINS THAT REQUIRED MANAGEMENT AT THE UNIVERSITY HOSPITAL PAIN CENTRE ARE ON THE LEFT, WHERE THE TWO PROSTHESES OVERLAP. RECURRENCE. QUALITY OF LIFE EXTREMELY DEGRADED. LIFE ON HOLD, AND IT IS GETTING WORSE. THESE PROSTHESES HAVE BEEN IN PLACE FOR 10 YEARS AND I HAVE BEEN STRUGGLING EVER SINCE. SOMETIMES THE PAIN LEVEL IS EXTREME. DAILY SUFFERING REQUIRING USE OF VERSATIS PATCHES, ANALGESICS, PSYCHOLOGICAL FOLLOW-UP. USE OF PERISTEEN PLUS LAXATIVES. ANTIHISTAMINES, ANXIOLYTICS AND HYPNOTICS. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Hernia; Pain

  MAUDE report 24283550 ↗
• InjuryFeb 4, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT HERNIA PROCEDURE ON (B)(6) 2010 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REVISION ON (B)(6) 2023. IT WAS REPORTED THAT THE PATIENT EXPERIENCED BULGING, INCISIONAL SCARS AND PAIN. NO ADDITIONAL INFORMATION WAS REPORTED.

  Patient problems: Pain; Scar Tissue; Swelling/ Edema

  MAUDE report 24258507 ↗
• InjuryFeb 3, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT PATIENT UNDERWENT LEFT INGUINAL HERNIA REPAIR ON (B)(6) 2015 AND A MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT REMOVAL SURGERY ON (B)(6) 2024. IT WAS REPORTED THAT THE PATIENT EXPERIENCED CHRONIC PAIN. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Pain

  MAUDE report 24245831 ↗
• InjuryJan 26, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT PATIENT UNDERWENT BILATERAL INGUINAL HERNIA REPAIR ON (B)(6) 2018 AND TWO MESHES WERE IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT RECURRENT LEFT HERNIA REPAIR ON (B)(6) 2019 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT RECURRENT BILATERAL INGUINAL HERNIA REPAIR ON (B)(6) 2020. IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN UNKNOWN ADVERSE EVENT. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS REPORTED.

  Patient problems: Hernia

  MAUDE report 24181739 ↗
• InjuryJan 26, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT PATIENT UNDERWENT BILATERAL INGUINAL HERNIA REPAIR ON (B)(6) 2018 AND TWO MESHES WERE IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT RECURRENT LEFT HERNIA REPAIR ON (B)(6) 2019 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT RECURRENT BILATERAL INGUINAL HERNIA REPAIR ON (B)(6) 2020. IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN UNKNOWN ADVERSE EVENT. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS REPORTED.

  Patient problems: Hernia

  MAUDE report 24181736 ↗
• InjuryJan 26, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT PATIENT UNDERWENT BILATERAL INGUINAL HERNIA REPAIR ON (B)(6) 2018 AND TWO MESHES WERE IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT RECURRENT LEFT HERNIA REPAIR ON (B)(6) 2019 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT RECURRENT BILATERAL INGUINAL HERNIA REPAIR ON (B)(6) 2020. IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN UNKNOWN ADVERSE EVENT. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS REPORTED.

  Patient problems: Hernia

  MAUDE report 24181735 ↗
• InjuryJan 26, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT PATIENT UNDERWENT BILATERAL INGUINAL HERNIA REPAIR ON (B)(6) 2018 AND TWO MESHES WERE IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT RECURRENT LEFT HERNIA REPAIR ON (B)(6) 2019 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT RECURRENT BILATERAL INGUINAL HERNIA REPAIR ON (B)(6) 2020. IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN UNKNOWN ADVERSE EVENT. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS REPORTED.

  Patient problems: Hernia

  MAUDE report 24181733 ↗
• InjuryJan 23, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT PATIENT UNDERWENT RECURRENT LEFT HERNIA REPAIR ON (B)(6) 2019 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT RECURRENT BILATERAL INGUINAL HERNIA REPAIR ON (B)(6) 2020. IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN UNKNOWN ADVERSE EVENT. IT WAS PREVIOUSLY REPORTED THAT THE PATIENT HAD UNDERWENT BILATERAL INGUINAL HERNIA REPAIR ON (B)(6) 2018 AND TWO MESH WERE IMPLANTED. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS REPORTED.

  Patient problems: Hernia

  MAUDE report 24171597 ↗
• InjuryJan 22, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT PATIENT UNDERWENT RIGHT INGUINAL HERNIA REPAIR ON (B)(6) 2022 AND A MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT REMOVAL SURGERY ON (B)(6) 2022. IT WAS REPORTED THAT THE PATIENT EXPERIENCED RIGHT GROIN PAIN. NO ADDITIONAL INFORMATION WAS REPORTED.

  Patient problems: Pain

  MAUDE report 24153781 ↗
• InjuryJan 20, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT INGUINAL HERNIA REPAIR ON (B)(6) 2022 AND MESH WAS IMPLANTED. FOLLOWING SURGERY, THE PATIENT REPORTED EXPERIENCING SEVERE RESIDUAL PAIN AFTER THIS REPAIR OF THE LEFT INGUINAL HERNIA. THE PAIN PREVENTED THE PATIENT FROM SITTING FOR MORE THAN 30 MINUTES, CAUSED NIGHTTIME PAIN, BACK PAIN, AND AN INABILITY TO PLAY SPORTS. THE PATIENT FURTHER REPORTED PUBALGIA, PAIN OF THE PUBIC SYMPHYSIS, ILIO-INGUINAL PAIN, AND SCIATICA WERE THE TERMS MOST OFTEN USED BY DOCTORS TO DESCRIBE THEIR SYMPTOMS. THE PATIENT HAD TO UNDERGO SEVERAL PELVIC MRIS AND ULTRASOUNDS, WHICH DID NOT REVEAL ANY ABNORMALITIES. THE PATIENT ATTENDED SESSIONS OF PHYSIOTHERAPY, OSTEOPATHY, AND CHINESE MEDICINE, HAD TWO INFILTRATIONS (INJECTIONS), AND ULTIMATELY WENT TO A PAIN EVALUATION AND TREATMENT CENTER (CEDT) TO RECEIVE TRANSCUTANEOUS ELECTRICAL NERVE STIMULATION (TENS) TREATMENT FOR SIX MONTHS. THIS LAST TREATMENT SUCCEEDED IN MAKING THE PAIN TOLERABLE AND MANAGEABLE. NO FURTHER INFORMATION IS AVAILABLE OR COULD BE OBTAINED AS REPORTER DETAILS HAVE NOT BEEN DISCLOSED (CONFIDENTIAL).

  Patient problems: Pain

  MAUDE report 24120638 ↗
• MalfunctionSep 9, 2025Material Integrity Problem; Material Integrity Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN UNKNOWN PROCEDURE IN 2025 AND MESH WAS USED. THE MESH CIRCLES WERE NOT SYMMETRICAL AS USUAL. THE SURGERY WAS NOT DELAYED DUE TO THE REPORTED EVENT. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23011430 ↗
• MalfunctionSep 9, 2025Material Integrity Problem; Material Integrity Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN UNKNOWN PROCEDURE IN 2025 AND MESH WAS USED. THE MESH CIRCLES WERE NOT SYMMETRICAL AS USUAL. THE SURGERY WAS NOT DELAYED DUE TO THE REPORTED EVENT. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23011429 ↗
• InjuryAug 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2012 AND A MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2013. IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN AND BULGING. NO ADDITIONAL INFORMATION WAS REPORTED.

  Patient problems: Pain; Swelling/ Edema

  MAUDE report 22696978 ↗
• InjuryJun 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT HERNIA REPAIR SURGERY (B)(6) 2012 AND A MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT EXPERIENCED PAIN. NO ADDITIONAL INFORMATION WAS REPORTED.

  Patient problems: Pain

  MAUDE report 22290470 ↗
• InjuryMay 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT OPEN RIGHT INGUINAL HERNIORRHAPHY WITH MESH ON (B)(6) 2015 AND A MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN UNKNOWN ADVERSE EVENT. NO ADDITIONAL INFORMATION WAS PROVIDED. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 22082927 ↗
• InjuryMay 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT LEFT AND RIGHT INGUINAL HERNIA REPAIR SURGERY ON (B)(6) 2009 AND TWO (2) MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT EXPERIENCED SCARRING AND PAIN. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: Pain; Scar Tissue

  MAUDE report 22068049 ↗
• InjuryMay 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT LEFT AND RIGHT INGUINAL HERNIA REPAIR SURGERY ON (B)(6) 2009 AND TWO (2) MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT EXPERIENCED SCARRING AND PAIN. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: Pain; Scar Tissue

  MAUDE report 22058987 ↗
• InjuryMay 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT INCISIONAL HERNIA REPAIR ON (B)(6) 2018 AND A MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT HERNIA REPAIR ON (B)(6) 2019 AND A MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: Pain

  MAUDE report 22058806 ↗