ULTRAPRO UPPM2Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705031132436), received between Aug 13, 2019 and Oct 4, 2022 — classified as 2 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryOct 4, 2022Adverse 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 VENTRAL INCISIONAL HERNIA, MULTIFOCAL REPAIR PROCEDURE ON (B)(6) 2008 AND MESH X3 WERE IMPLANTED. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REVISION ON (B)(6) 2009 DUE TO RECURRENT VENTRAL INCISIONAL HERNIA, PAIN AND ADHESIONS. THE PATIENT HAD A PREVIOUS MESH IMPLANTED ON (B)(6) 2007 WHICH IS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Adhesion(s); Hernia; Pain

  MAUDE report 15541353 ↗
• InjuryAug 13, 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 BILATERAL INGUINAL HERNIA REPAIR SURGERY ON (B)(6) 2015 AND TWO MESH PRODUCTS WERE IMPLANTED. NO ADDITIONAL INFORMATION IS PROVIDED.

  Patient problems: Injury

  MAUDE report 8887260 ↗