ES™ TROCHANTERIC NAIL, RIGHT, Ø11mm x 39cm x 125° 1023-395Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00848665014532), received between Oct 30, 2023 and Oct 30, 2023 — classified as 1 injury.

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 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 30, 2023Break; Break

  ON (B)(6) 2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT A PATIENT UNDERWENT SURGERY DUE TO AN INTERTROCHANTERIC FRACTURE IN (B)(6) 2023. ON 10/4/2023, THE SALES REPRESENTATIVE WAS MADE AWARE VIA PHONE THAT THE LAG SCREW IMPLANTED IN THE PATIENT BROKE. THE PATIENT WILL UNDERGO REVISION SURGERY. NO FURTHER INFORMATION HAS BEEN PROVIDED. ADDITIONAL INFORMATION RECEIVED ON 10/13/2023: IN (B)(6) 2023, THE PATIENT UNDERWENT SURGERY IN WHICH A 1023-395 TROCHANTERIC NAIL AND A 1099-095 LAG SCREW WERE IMPLANTED. ON (B)(6) 2023, THE PATIENT FELT PAIN WHILE WALKING. A REVISION SURGERY TOOK PLACE ON 10/6/2023 TO REMOVE THE TROCH NAIL AND LAG SCREW. DURING THE REMOVAL OF THE LAG SCREW, IT WAS NOTICED THAT IT HAD SCRATCHES DISTAL TO THE THREADS. THE CASE WAS COMPLETED AS A TOTAL HIP ARTHROPLASTY PROCEDURE.

  Patient problems: Pain

  MAUDE report 18029143 ↗