DM Converter – TiN coated 01.32.3844CFRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630971256354), received between Mar 31, 2026 and Mar 31, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.

• InjuryMar 31, 2026Device Dislodged or Dislocated

  THE PATIENT HAD PRIMARY SURGERY ON (B)(6) 2020. ON (B)(6) 2026, THE PATIENT CAME IN DUE TO A DISLOCATION OF THE HEAD AND LINER AS THE RESULT OF A FALL. THE SURGEON REVISED THE 36MM HEAD AND D 36 LINER TO A 28MM HEAD AND D 28 LINER. THE SURGERY WAS COMPLETED SUCCESSFULLY. PRESENTLY, ON (B)(6) 2026, THE PATIENT CAME IN PRESENTING PAIN DUE TO A DISLOCATION OF THE DM LINER AND DM CONVERTER. THE CAUSE IS UNKNOWN AS NO TRAUMA WAS REPORTED. THE SURGEON REVISED THE DM BIOLOX D 28 LINER TO A FACE CHANG 10° PE HD LINER D 36 AND REVISED THE 28MM BIOLOX DELTA HEAD M TO A 36MM BIOLOX DELTA HEAD XL. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Joint Dislocation

  MAUDE report 24738822 ↗