ULTRAPRO UPPS6Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10705031132603), received between Feb 12, 2019 and Nov 20, 2024 — classified as 5 injuries.

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryNov 20, 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 REPAIR OF RECURRENT VENTRAL HERNIA SURGERY ON (B)(6) 2012 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REPAIR OF VENTRAL HERNIA AND EXCISION OF PREVIOUSLY PLACED MESH ON (B)(6) 2020. IT WAS REPORTED THAT THE PATIENT EXPERIENCED UNDISCLOSED INJURY. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 20732178 ↗
• InjurySep 17, 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) 2013 AND AN MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2013 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REPAIR OF EPIGASTRIC AND INFRAUMBILICAL HERNIA ON (B)(6) 2016 AND TWO MESH WERE IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT RECURRENT INGUINAL HERNIA REPAIR SURGERY ON (B)(6) 2017 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN, RIGHT GROIN PAIN AND BULGE. IT WAS PREVIOUSLY REPORTED THAT THE PATIENT HAD RECURRENT HERNIA REPAIR ON (B)(6) 2012 AND MESH WAS IMPLANTED. OTHER PROCEDURES WERE CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Pain; Swelling/ Edema

  MAUDE report 20242005 ↗
• InjurySep 17, 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) 2013 AND AN MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2013 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REPAIR OF EPIGASTRIC AND INFRAUMBILICAL HERNIA ON (B)(6) 2016 AND TWO MESH WERE IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT RECURRENT INGUINAL HERNIA REPAIR SURGERY ON (B)(6) 2017 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN, RIGHT GROIN PAIN AND BULGE. IT WAS PREVIOUSLY REPORTED THAT THE PATIENT HAD RECURRENT HERNIA REPAIR ON (B)(6) /2012 AND MESH WAS IMPLANTED. OTHER PROCEDURES WERE CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Pain; Swelling/ Edema

  MAUDE report 20242002 ↗
• InjurySep 17, 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) 2013 AND AN MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2013 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT REPAIR OF EPIGASTRIC AND INFRAUMBILICAL HERNIA ON (B)(6) 2016 AND TWO MESH WERE IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT RECURRENT INGUINAL HERNIA REPAIR SURGERY ON (B)(6) 2017 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN, RIGHT GROIN PAIN AND BULGE. IT WAS PREVIOUSLY REPORTED THAT THE PATIENT HAD RECURRENT HERNIA REPAIR ON (B)(6) 2012 AND MESH WAS IMPLANTED. OTHER PROCEDURES WERE CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Hernia; Pain; Swelling/ Edema

  MAUDE report 20237821 ↗
• InjuryFeb 12, 2019Adverse 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 MESHX2 WERE IMPLANTED. IT WAS REPORTED THE PATIENT EXPERIENCED AN UNDISCLOSED ADVERSE EVENT. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Injury

  MAUDE report 8330530 ↗