ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193109Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304697911), received between Apr 5, 2022 and May 12, 2023 — 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.

• InjuryMay 12, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT WAS SEEN FOR BURSITIS AND TREATED WITH FORMAL PHYSICAL THERAPY AND OVER THE COUNTER TOPICAL CREAM FOR ONGOING PAIN. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Bursitis; Cellulitis; Pain; Swelling/ Edema; Unspecified Infection

  MAUDE report 16918479 ↗
• InjuryApr 5, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED DURING AN INITIAL PROCEDURE THAT A GREATER TROCHANTERIC FRACTURE NONDISPLACED NOTED AT TIME OF SURGERY AND ON POSTOPERATIVE X-RAY. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Bone Fracture(s)

  MAUDE report 14015318 ↗