Dyna Locking Trochanteric Nail™ NG1120Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 08800015916509), received between Aug 21, 2018 and Dec 3, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (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 16, 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.

• InjuryDec 3, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THIS EVENT OCCURED IN SOUTH KOREA. THE FEMALE PATIENT UNDERWENT SURGERY FOR IMPLANTING DYNA LOCKING TROCHANTERIC NAIL SYSTEM ON (B)(6) 2018. IT IS CONFIRMED THAT THE TROCHANTERIC NAIL 130-11X200MM(NG1120) HAS BEEN BROKEN IN THE PATIENT BODY POSTOPERATIVELY AFTER AROUND 10 MONTHS ((B)(6) 2019) AND THE REVISION SURGERY WAS CONDUCTED FOR REMOVING THE NAIL ((B)(6) 2019).

  Patient problems: Pain

  MAUDE report 9400194 ↗
• InjuryAug 21, 2018Break; Break

  THIS EVENT OCCURRED IN (B)(6). A PATIENT UNDERWENT SURGERY ON (B)(6) 2018. A 130-11X200MM TROCHANTERIC NAIL WAS BROKEN IN PATIENT POSTOPERATIVELY. THE BROKEN TROCHANTERIC NAIL WAS REMOVED AND REPLACED WITH ANOTHER PRODUCTS ON (B)(6) 2018. IT WAS REPORTED THAT AFTER REVISION SURGERY, THE PATIENT LEFT THE HOSPITAL AS GOOD.

  Patient problems: Pain

  MAUDE report 7800186 ↗