Dall-Miles 6704-3-081Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540568106), received between Jul 12, 2018 and Jul 12, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (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.

• InjuryJul 12, 2018Migration; Migration

  AS REPORTED: "CHRONIC DISLOCATIONS, CONSTRAINED LINER DAMAGE DURING DISLOCATION. [DALL MILES] PLATE REMOVED"; LEFT HIP. UPDATE 14 JUNE, 2018: THE MEDICAL REVIEW HAS CONFIRMED THAT THE CONSTRAINED LINER HAS DISASSOCIATED FROM AN UNKNOWN TRIDENT SHELL. IT HAS ALSO CONFIRMED LOOSENING OF THE DALL MILES PLATE. THE CONCLUSION OF THE ASSESSMENT IS AS FOLLOWS: "NON-UNION OF A GREATER TROCHANTERIC FRACTURE, PRESENT ALREADY BEFORE IMPLANTATION OF THE PREDICATE DEVICES AFTER A PERIPROSTHETIC FRACTURE DUE TO A FALL OF THE PATIENT IN 2015, DESPITE ADEQUATE TREATMENT, HAS CONTRIBUTED TO AN OVERLOAD CONDITION ON THE IMPLANTED CONSTRAINED LINER FORCING A COMPLETE PULL-OUT OF THE CONSTRAINED LINER FROM THE CUP SHELL REQUIRING A THIRD REVISION IN (B)(6) 2018". UPDATE 18 JUNE 18: A REVIEW BY A CLINICAL CONSULTANT HAS CONFIRMED A FRACTURED DALL MILES CABLE.

  Patient problems: Bone Fracture(s); Injury; Joint Dislocation

  MAUDE report 7681399 ↗