ECHO BI-METRIC MICROPLASTY HIP SYSTEM 193013Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304697805), received between Dec 19, 2019 and Jan 24, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (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.
Reports received per month
Most reported problems
Device problems
- Loss of or Failure to Bond1
- Positioning Failure1
- Unstable1
Patient problems
- Bone Fracture(s)1
- Fall1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 24, 2025Positioning Failure; Positioning Failure
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE. DURING THE PROCEDURE, THE SURGEON BROACHED TO A SIZE 13 FEMORAL STEM; HOWEVER, WHEN PLACING THE FINAL STEM, THE SURGEON NOTED THAT THERE WAS NOT ENOUGH BONE SUPPORT SURROUNDING THE UNCEMENTED STEM, AND THE FIT OF THE IMPLANT WAS INADEQUATE. THE STEM WAS REMOVED. THE PROCEDURE WAS COMPLETED WITH A NEW STEM. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21229914 ↗InjuryDec 19, 2019Loss of or Failure to Bond; Unstable; Loss of or Failure to Bond; Unstable
NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.
Patient problems: Bone Fracture(s); Fall
MAUDE report 9494579 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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