ECHO FX HIP SYSTEM 12-151409Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00880304520295), received between Aug 17, 2026 and Aug 17, 2026 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Pain1
- Swelling/ Edema1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 17, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the patient underwent an initial right total hip arthroplasty. Subsequently, the patient underwent a head and liner exchange approximately 2 years and 4 months post-implantation due to trunnionosis and metal-related pathology. The patient reported ongoing extreme pain and swelling following the revision. Attempts have been made and no further information has been provided.
Patient problems: Pain; Swelling/ Edema
MAUDE report 50274685 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.