ULTRAPRO ADVANCED UPA1515Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705031236967), received between Jan 21, 2020 and Jul 20, 2020 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Packaging 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

• InjuryJul 20, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT A VENTRAL HERNIA REPAIR ON AN UNKNOWN DATE IN 2019 AND THE MESH WAS IMPLANTED. IT WAS REPORTED THE PATIENT EXPERIENCED A POST OP MRSA INFECTION. IT WAS ALSO REPORTED THAT THE DEVICE WAS REMOVED AND THE WOUND WAS CLEANED.

  Patient problems: Bacterial Infection; Not Applicable

  MAUDE report 10299263 ↗
• MalfunctionJan 21, 2020Packaging Problem; Packaging Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN INGUINAL HERNIA REPAIR PROCEDURE ON (B)(6) 2019 AND THE MESH WAS IMPLANTED. IT WAS REPORTED THAT THE TOP LEFT SIDE OF THE PACKAGING DID NOT APPEAR TO BE SEALED ALL THE WAY. A LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9612660 ↗