ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193110Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00880304697928), received between Dec 2, 2021 and Dec 2, 2021 — classified as 1 malfunction.

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

• MalfunctionDec 2, 2021Positioning Failure; Positioning Failure

  IT WAS REPORTED WHILE CANAL BROACHING, SURGEON SEQUENTIALLY BROACHED FROM 7MM UP TO 10MM WITH ZB ECHO MICRO BROACHES, AS WELL AS TRIALING. HE FELT THE 10MM BROACH WAS THE CORRECT SIZE, FIT AND FILL. HE ASKED FOR THE 10MM ECHO MICRO IMPLANT. THE 10MM IMPLANT SUBSIDED. SURGERY WAS COMPLETED WITH A 11MM ECHO MICRO IMPLANT. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12915230 ↗