ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193112Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304697942), received between Apr 1, 2021 and Mar 5, 2024 — classified as 2 injuries.

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMar 5, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THE PATIENT UNDERWENT A LEFT HIP REVISION APPROXIMATELY 18 MONTHS POST IMPLANTATION DUE TO PAIN. ALL THE COMPONENTS WERE REMOVED AND REPLACED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Pain

  MAUDE report 18837996 ↗
• InjuryApr 1, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THE PATIENT UNDERWENT INITIAL LEFT TOTAL HIP ARTHROPLASTY. APPROXIMATELY 7 MONTHS POSTOP, THE PATIENT REPORTED SEVERE ANTERIOR THIGH PAIN RESULTING IN DAILY TRAMADOL USE. RESOLVED APPROXIMATELY 2 YEARS AND 3 MONTHS POST IMPLANTATION AFTER THE PATIENT UNDERWENT LEFT CORTICAL PERIOSTEAL ABLATION/DEBRIDEMENT. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

  Patient problems: Pain

  MAUDE report 11606664 ↗