Dyna Locking Trochanteric Nail™ NGA2100Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08800015918060), received between Oct 6, 2020 and Oct 6, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Migration or Expulsion of Device” (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.

• InjuryOct 6, 2020Migration or Expulsion of Device; Migration or Expulsion of Device

  AFTER UNDERGOING TROCHANTERIC NAIL INSERTION SURGERY ON (B)(6) 2020, THE PATIENT STARTED TO FEEL PAIN IN THE SURGERY AREA. SUBSEQUENTLY THE PATIENT VISITED THE HOSPITAL ON (B)(6) 2020 AND IT WAS CONFIRMED THAT CUT-OUT WAS OBSERVED AS THE NECK SCREW ENTERED ACETABULUM. THE RELEVANT IMPLANTS WERE REMOVED ON (B)(6) 2020 THEN TOTAL HIP REPLACEMENT WAS PERFORMED ON THE PATIENT IN THE OTHER HOSPITAL.

  Patient problems: Pain

  MAUDE report 10639771 ↗