ULTRAPRO UPPS2Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10705031132443), received between Oct 4, 2022 and Mar 12, 2025 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (1 report).

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMar 12, 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 OF RIGHT INGUINAL HERNIA AND MESH WAS IMPLANTED ON (B)(6) 2011. IT WAS REPORTED THAT THE PATIENT UNDERWENT LAPAROSCOPIC VENTRAL HERNIA REPAIR AND MESH WAS IMPLANTED ON (B)(6) 2011. NO OTHER INFORMATION WAS PROVIDED. OTHER PROCEDURE WAS CAPTURED IN A SEPARATE FILE. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 21590561 ↗
• MalfunctionMar 3, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT A CUSTOMER CALLED RECEIVED MESH PRODUCT ON AN UNKNOWN DATE AND THE EXTERIOR DID NOT HAVE THE USUAL LABELS, THEY WERE MISSING. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16480293 ↗
• 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 15541355 ↗