Accolade 6057-0537DRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327020694), received between Feb 2, 2021 and Apr 28, 2025 — classified as 2 injuries.

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. 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.

• InjuryApr 28, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT REPORTS "SOMETHING SNAPPED" AND CONTINUOUS DISCOMFORT IN HIS STRYKER TOTAL HIP REPLACEMENT. PATIENT ALSO IS INQUIRING WHETHER HIS IMPLANTS HAVE BEEN SUBJECT TO A RECALL.

  Patient problems: Discomfort

  MAUDE report 21922055 ↗
• InjuryFeb 2, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: "DR...PERFORMED A LEFT HIP REVISION DUE TO INFECTION. ALL EXPLANTED IMPLANTS ARE MARKED ON ATTACHMENT." REP CONFIRMED THAT EXPLANTS ARE NOT AVAILABLE FOR RETURN DUE TO HOSPITAL POLICY AND NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Unspecified Infection

  MAUDE report 11267960 ↗