Dall-Miles 3704-2-082Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613154490271), received between May 4, 2021 and May 4, 2021 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMay 4, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THIS PI IS FOR THE REMOVAL OF CABLES AND A PLATE ON (B)(6) 2015. IN PROVIDING INFORMATION FOR A REVISION OF THE PATIENT'S LEFT HIP ON (B)(6) 2021, AN OPERATIVE REPORT FOR 16/NOVEMBER/2015 WAS PROVIDED WHICH NOTES: "...UNDERWENT REVISION OF HIS...HIP REPLACEMENT IN (B)(6) 2015. HE HAS DEVELOPED SIGNIFICANT PAIN WHICH SEEMS TO BE ASSOCIATED WITH A TROCHANTERIC PLATE AND CABLES IMPLANTED TO TREAT AN INTRAOPERATIVE PROXIMAL FEMUR FRACTURE...THE FRACTURE DID NOT DISPLACE AND APPEARS TO HAVE HEALED..." ALL CABLES AND A PLATE WERE REMOVED. SPOKE TO THE REP WHO WAS PRESENT FOR THE (B)(6) 2015 REVISION. THE REP WAS NOT INFORMED OF AN INTRA-OPERATIVE FRACTURE AND WASN'T AWARE IF THE ADDITIONAL HARDWARE WAS BEING PLACED PROPHYLACTICALLY. FURTHERMORE, THE REP CONFIRMED HE WAS NOT PRESENT FOR THE PROCEDURE TO REMOVE THE PLATE AND CABLES, AND CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Pain

  MAUDE report 11770425 ↗