Offset stem adapter 2903-3020Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04712771509908), received between May 24, 2018 and May 25, 2018 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (2 reports).

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.

• InjuryMay 25, 2018Break; Break

  IT WAS REPORTED TO UOC THAT A PATIENT WHO HAD UNDERGONE A PRIOR KNEE REVISION SURGERY, HAD TO BE REVISED. IN THE REVISION, THE SURGEON REMOVED A BROKEN DEVICE AND IMPLANTED NEW REVISION COMPONENTS.

  Patient problems: Bone Fracture(s)

  MAUDE report 7546985 ↗
• InjuryMay 24, 2018Break

  IT WAS REPORTED TO UOC THAT A PATIENT WHO HAD UNDERGONE A PRIOR KNEE REVISION SURGERY, HAD TO BE REVISED. IN THE REVISION, THE SURGEON REMOVED A BROKEN DEVICE AND IMPLANTED NEW REVISION COMPONENTS.

  Patient problems: No Code Available

  MAUDE report 7542745 ↗