ETHICON PHYSIOMESH PHY1015VRecalls & reported problems

Summary

The FDA's MAUDE database contains 81 adverse event reports that list this exact device (DI 10705031132306), received between Dec 4, 2017 and Jul 3, 2025 — classified as 81 injuries.

The most frequently reported specific device problem is “Migration” (2 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 81 reports, in the reporter's own words as published by the FDA.

• InjuryJul 3, 2025Material Integrity Problem; Adverse Event Without Identified Device or Use Problem; Material Integrity Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN UMBILICAL HERNIA REPAIR PROCEDURE ON (B)(6) 2014 AND MESH WAS IMPLANTED FOR PARIETAL REINFORCEMENT TYPE. FOLLOWING THIS OPERATION, THE PATIENT BEGAN TO HAVE PAIN AND WAS CONSULTED AGAIN. THE PATIENT UNDERWENT A SECOND OPERATION ON (B)(6) 2016. DURING THIS ONE, THE SURGEON DISCOVERED THAT PART OF THE FIRST PARIETAL REINFORCEMENT HAD DETACHED AND A NEW HERNIA AT THE LEVEL OF THE WHITE LINE. THE PATIENT WAS IMPLANTED WITH A SECOND REINFORCEMENT (NOT A J&J DEVICE) DURING THIS SECOND OPERATION. CURRENT STATE OF THE PATIENT: AFTER THE FIRST OPERATION, THE PATIENT FELT ABDOMINAL PAIN THAT THEY THOUGHT WAS DUE TO THE FORMATION OF THE NEW HERNIA AND THE FACT THAT THE PROSTHESIS HAD COME OFF. BUT IT REALLY FOLLOWED THE SECOND OPERATION THAT THE PATIENT STARTED TO HAVE ABDOMINAL PAIN, THEN AT THE HIP, THEN AT THE BACK. THE PATIENT SUFFERS FROM CHRONIC AND DISABLING PAIN IN DAILY LIFE. THE DIFFERENT TREATMENTS PUT IN PLACE FOR THESE PAINS ARE WITHOUT GREAT RESULTS, THE PAINS ARE DAILY. NO FURTHER INFORMATION IS AVAILABLE OR COULD BE OBTAINED AS REPORTER DETAILS HAVE NOT BEEN DISCLOSED (CONFIDENTIAL).

  Patient problems: Hernia; Pain; Seroma; Swelling/ Edema

  MAUDE report 22395086 ↗
• InjuryMay 16, 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 REPAIR INCISIONAL HERNIA AND A MESH WAS IMPLANTED ON (B)(6) 2015. IT WAS REPORTED THAT THE PATIENT UNDERWENT OPEN VENTRAL HERNIA REPAIR AND A MESH WAS IMPLANTED ON (B)(6) 2016. IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN UNKNOWN ADVERSE EVENT. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 22034512 ↗
• InjuryMay 6, 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 REMOVAL SURGERY AND MESH WAS IMPLANTED ON (B)(6) 2014. IT WAS REPORTED THAT THE PATIENT HAD UNDERWENT HERNIA PROCEDURE AND MESH WAS IMPLANTED ON (B)(6) 2007. IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN UNKNOWN ADVERSE EVENT. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 21968348 ↗
• InjuryApr 23, 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 ON (B)(6) 2014 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2023 DURING WHICH THE SURGEON NOTED DENSE ADHESIONS NEAR THE UMBILICUS FROM HIS PREVIOUS HERNIA SURGERY. THESE WERE TEDIOUSLY TAKEN DOWN UNTIL THE ENTIRE SMALL BOWEL COULD BE RUN. AT THE ILEOCECAL VALVE, THERE WAS AN OBSTRUCTION WITH AN ASSOCIATED MASS AT THE MESENTERIC BORDER. THIS AREA OF THE SMALL BOWEL WAS RESECTED FOR A DISTANCE OF APPROXIMATELY 12 INCHES OF SMALL BOWEL. IT WAS REPORTED THAT THE PATIENT EXPERIENCED SEVERE PAIN, SMALL BOWEL OBSTRUCTION WITH RESECTIONING, AND ADHESIONS. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: Adhesion(s); Hernia; Obstruction/Occlusion; Pain

  MAUDE report 21896671 ↗
• InjuryJan 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 HERNIA REPAIR SURGERY ON (B)(6)2015 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6)2023. IT WAS REPORTED PATIENT EXPERIENCED SEVERE PAIN, NAUSEA, DIARRHEA, CHILLS, INFLAMMATION, AND A SMALL BOWEL OBSTRUCTION. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Chills; Diarrhea; Inflammation; Nausea; Obstruction/Occlusion; Pain

  MAUDE report 21195467 ↗
• InjuryJan 14, 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 REMOVAL SURGERY ON (B)(6) 2015 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED ABDOMINAL PAIN, SMALL-BOWEL OBSTRUCTION, AND NAUSEA. IT WAS PREVIOUSLY REPORTED THAT THE PATIENT HAD HERNIA REPAIR ON (B)(6) 2010, (B)(6) 2011, AND ON (B)(6) 2012. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Abdominal Pain; Nausea; Obstruction/Occlusion

  MAUDE report 21147328 ↗
• InjuryJan 8, 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 HERNIA REPAIR ON (B)(6) 2012 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REMOVAL SURGERY ON (B)(6) 2023. IT WAS REPORTED THAT PATIENT EXPERIENCED SEVERE PAIN, NAUSEA, DIARRHEA, CHILLS, INFLAMMATION, LOSS OF APPETITE, AND EXTREME WEIGHT LOSS. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Chills; Decreased Appetite; Diarrhea; Inflammation; Nausea; Pain; Weight Changes

  MAUDE report 21099980 ↗
• InjuryDec 12, 2024Adverse 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 PROCEDURE ON (B)(6) 2015 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2023. IT WAS REPORTED THAT THE PATIENT EXPERIENCED SEVERE PAIN, NAUSEA, DIARRHEA, CHILLS, INFLAMMATION, AND A SMALL BOWEL OBSTRUCTION. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Chills; Diarrhea; Inflammation; Nausea; Obstruction/Occlusion; Pain

  MAUDE report 20921514 ↗
• InjuryDec 2, 2024Adverse 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 ON (B)(6) 2015 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED DISCOMFORT, BULGE, PAIN, AND ADHESIONS. IT WAS REPORTED THAT THE PATIENT HAD AN HERNIA REPAIR ON (B)(6) 2015 AND MESH WAS IMPLANTED. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Adhesion(s); Discomfort; Pain; Swelling/ Edema

  MAUDE report 20819140 ↗
• InjuryNov 26, 2024Adverse 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 REMOVAL SURGERY AND RECURRENT HERNIA REPAIR SURGERY ON (B)(6) 2014 AND MESH WAS IMPLANTED. THE PATIENT EXPERIENCED UNDISCLOSED INJURY. NO OTHER INFORMATION PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 20782158 ↗
• InjuryNov 26, 2024Adverse 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 RECURRENT HERNIA REPAIR SURGERY ON (B)(6) 2015 AND MESH WAS IMPLANTED. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 20781531 ↗
• InjuryNov 11, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY AN ATTORNEY THAT PATIENT UNDERWENT HERNIA REPAIR ON (B)(6) 2017 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED OBSTRUCTION AND ADHESION. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Adhesion(s); Obstruction/Occlusion

  MAUDE report 20651769 ↗
• InjuryNov 7, 2024Adverse 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 PROCEDURE ON (B)(6) 2021 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REMOVAL SURGERY ON (B)(6) 2023. IT WAS REPORTED THAT THE PATIENT EXPERIENCED SEVERE PAIN, NAUSEA, DIARRHEA, CHILLS, INFLAMMATION, AND A SMALL BOWEL OBSTRUCTION. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Chills; Diarrhea; Inflammation; Nausea; Obstruction/Occlusion; Pain

  MAUDE report 20627195 ↗
• InjuryNov 5, 2024Adverse 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 AND REMOVAL SURGERY ON (B)(6) 2012 AND MESH WAS IMPLANTED. OTHER PROCEDURE WAS CAPTURED IN ANOTHER FILE. NO ADDITIONAL INFORMATION PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 20607737 ↗
• InjuryOct 23, 2024Adverse 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 ON (B)(6) 2016 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REVISION ON (B)(6) 2017 DUE TO ABDOMINAL PAIN AND NAUSEA. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REVISION ON (B)(6) 2017 DUE TO WOUND INFECTION AND ABDOMINAL CELLULITIS. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REMOVAL ON (B)(6) 2018 DUE INFECTED INCISIONAL HERNIA, ABSCESS AND ADHESIONS. IT WAS REPORTED THAT THE PATIENT EXPERIENCED HERNIA RECURRENCE, PAIN, AND ADHESIONS. THE PATIENT HAD A PREVIOUS MESH IMPLANTED ON (B)(6) 2012 WHICH IS CAPTURED IN SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Adhesion(s); Cellulitis; Hernia; Pain; Unspecified Infection

  MAUDE report 20519521 ↗
• InjuryOct 23, 2024Adverse 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 ON (B)(6) 2016 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REVISION ON (B)(6) 2017 DUE TO ABDOMINAL PAIN AND NAUSEA. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REVISION ON (B)(6) 2017 DUE TO WOUND INFECTION AND ABDOMINAL CELLULITIS. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REMOVAL ON (B)(6) 2018 DUE INFECTED INCISIONAL HERNIA, ABSCESS AND ADHESIONS. IT WAS REPORTED THAT THE PATIENT EXPERIENCED HERNIA RECURRENCE, PAIN, AND ADHESIONS. THE PATIENT HAD A PREVIOUS MESH IMPLANTED ON (B)(6) 2012 WHICH IS CAPTURED IN SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Abdominal Pain; Adhesion(s); Hernia; Nausea; Pain

  MAUDE report 20519513 ↗
• InjuryOct 23, 2024Adverse 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 ON (B)(6) 2016 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REVISION ON (B)(6) 2017 DUE TO ABDOMINAL PAIN AND NAUSEA. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REVISION ON (B)(6) 2017 DUE TO WOUND INFECTION AND ABDOMINAL CELLULITIS. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REMOVAL ON (B)(6) 2018 DUE INFECTED INCISIONAL HERNIA, ABSCESS AND ADHESIONS. IT WAS REPORTED THAT THE PATIENT EXPERIENCED HERNIA RECURRENCE, PAIN, AND ADHESIONS. THE PATIENT HAD A PREVIOUS MESH IMPLANTED ON (B)(6) 2012 WHICH IS CAPTURED IN SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Abscess; Adhesion(s); Hernia; Pain; Unspecified Infection

  MAUDE report 20517130 ↗
• InjuryOct 13, 2024Adverse 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 A HERNIA REPAIR PROCEDURE ON (B)(6) 2014 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REMOVAL SURGERY ON 6/11/2011. IT WAS REPORTED THAT THE PATIENT EXPERIENCED SEVERE PAIN, NAUSEA, DIARRHEA, CHILLS, INFLAMMATION, LOSS OF APPETITE, AND EXTREME WEIGHT LOSS. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Chills; Decreased Appetite; Diarrhea; Inflammation; Nausea; Pain; Weight Changes

  MAUDE report 20436522 ↗
• InjuryOct 13, 2024Adverse 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 ON (B)(6) 2012 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REPAIR ON (B)(6)2016 DUE TO INCARCERATED VENTRAL HERNIA AND PARTIAL BOWEL OBSTRUCTIONS. THE PATIENT EXPERIENCED NAUSEA, VOMITING, AND CRAMPY ABDOMINAL PAIN. IT WAS REPORTED THAT THE PATIENT UNDERWENT RECURRENT INCISIONAL HERNIA ON (B)(6)2017 AND MESH WAS IMPLANTED. THE PATIENT EXPERIENCED NAUSEA, VOMITING, AND CRAMPY ABDOMINAL PAIN. NO ADDITIONAL INFORMATION WAS PROVIDED. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Abdominal Pain; Cramp(s) /Muscle Spasm(s); Hernia; Nausea; Vomiting

  MAUDE report 20436520 ↗
• InjuryOct 11, 2024Adverse 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 REVISION SURGERY ON (B)(6) 2012 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REMOVAL SURGERY ON (B)(6) 2023 DURING WHICH THE SURGEON NOTED HE TOOK DOWN THE ENTEROCUTANEOUS FISTULA, SPENT SIGNIFICANT TIME LYSING ADHESIONS, RESECTED THREE PORTIONS OF THE SMALL BOWEL, REMOVED THE INFECTED MESH AND PERFORMED AN ABDOMINAL WALL RECONSTRUCTION. IT WAS REPORTED THAT THE PATIENT EXPERIENCED SEVERE PAIN, INFLAMMATION, INFECTION AND BOWEL RESECTION. IT WAS REPORTED THAT THE PATIENT HAD UNDERWENT A HERNIA REPAIR PROCEDURE ON (B)(6) 2012 AND MESH WAS IMPLANTED. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Adhesion(s); Fistula; Inflammation; Pain; Unspecified Infection

  MAUDE report 20428686 ↗
• InjuryOct 10, 2024Adverse 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 ON (B)(6) 2012 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REPAIR ON (B)(6) 2016 DUE TO INCARCERATED VENTRAL HERNIA AND PARTIAL BOWEL OBSTRUCTIONS. THE PATIENT EXPERIENCED NAUSEA, VOMITING, AND CRAMPY ABDOMINAL PAIN. IT WAS REPORTED THAT THE PATIENT UNDERWENT RECURRENT INCISIONAL HERNIA ON (B)(6)2017 AND MESH WAS IMPLANTED. THE PATIENT EXPERIENCED NAUSEA, VOMITING, AND CRAMPY ABDOMINAL PAIN. NO ADDITIONAL INFORMATION WAS PROVIDED. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Abdominal Pain; Cramp(s) /Muscle Spasm(s); Hernia; Nausea; Obstruction/Occlusion; Vomiting

  MAUDE report 20424099 ↗
• InjurySep 24, 2024Adverse 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 PROCEDURE ON (B)(6)2010 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6)2022. IT WAS REPORTED THE PATIENT EXPERIENCED ADHESIONS. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Adhesion(s)

  MAUDE report 20297876 ↗
• InjurySep 2, 2024Adverse 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 PROCEDURE ON (B)(6) 2013 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2023. IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN, NAUSEA, DIARRHEA, CHILLS, INFLAMMATION AND SMALL BOWEL OBSTRUCTION. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Chills; Diarrhea; Inflammation; Nausea; Obstruction/Occlusion; Pain

  MAUDE report 20118345 ↗
• InjuryAug 21, 2024Adverse 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 ON (B)(6) 2012 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT HERNIA REPAIR ON (B)(6) 2013. IT WAS REPORTED THAT PATIENT HAD HERNIA REPAIR SURGERY ON (B)(6) /2012 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN, HERNIA, ADHESIONS, AND OTHER UNDISCLOSED INJURY. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Adhesion(s); Hernia; Pain

  MAUDE report 20021314 ↗
• InjuryMay 26, 2024Adverse 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 ON (B)(6) 2014 AND TWO (2) MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN UNKNOWN ADVERSE EVENT. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 19399206 ↗