Titan™ HDL096006501Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780237051), received between Jun 10, 2022 and Jun 10, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJun 10, 2022Fracture; Fracture

  IT WAS REPORTED THAT, DURING REVERSE SHOULDER SURGERY, A GLENOSPHERE INSERTER BROKE INSIDE THE PATIENT. THE BROKEN PIECE WAS BURIED IN THE IMPLANT AND COULD NOT BE RETRIEVED. A FINISHING IMPACTOR WAS USED INSTEAD TO FULLY SEAT THE IMPLANT. NO DELAY WAS CAUSED AS A CONSEQUENCE OF THIS PROBLEM. NO FURTHER COMPLICATIONS WERE REPORTED.

  Patient problems: Foreign Body In Patient

  MAUDE report 14655116 ↗