Accolade 6720-1040Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540664532), received between Nov 8, 2017 and Nov 8, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. How this data works · Data updated Oct 13, 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.

• InjuryNov 8, 2017Insufficient Device Problem Information; Insufficient Device Problem Information

  SURGEON REPORTED THAT A PATIENT STATUS, POST LEFT TOTAL HIP DONE ON (B)(6) 2017, FELT A POP IN THE HIP AND COULD NOT BEAR WEIGHT. AN X-RAY WAS PERFORMED WHICH REVEALED A PERIPROSTHETIC FRACTURE OF THE FEMORAL CALCAR. SURGEON DECIDED TO REVISE THE HIP TO A RESTORATION MODULAR HIP STEM. THE FRACTURE WAS REDUCED, THE RESTORATION MODULAR HIP STEM WAS IMPLANTED PER SURGICAL TECHNIQUE. SEVERAL CABLE WERE APPLIED. A TRIAL REDUCTION WAS PERFORMED, SATISFIED WITH THE STABILITY AND LEG LENGTH, A FINAL HEAD WAS IMPACTED AND SURGICAL SITE WAS CLOSED. SURGERY WAS PERFORMED WITHOUT INCIDENCE.

  Patient problems: Bone Fracture(s); Injury

  MAUDE report 7011828 ↗