TMJ SYSTEM 01-6550TIRecalls & reported problems
Biomet Microfixation, Inc · 50 MM RIGHT NARROW TITANIUM MANDIBULAR COMPONENT · Class 3 · Implant
- 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 00841036081799), received between May 30, 2023 and Oct 17, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
17 other recalls cover devices cleared under the same FDA submission (P020016); they may or may not involve this specific model.
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
- Insufficient Device Problem Information1
Patient problems
- Insufficient Information2
- Skin Inflammation/ Irritation1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryOct 17, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT THE PATIENT UNDERWENT A RIGHT SIDE TMJ REPLACEMENT PROCEDURE APPROXIMATELY 2 YEARS AGO. APPROXIMATELY 7 MONTHS LATER, THE PATIENT UNDERWENT A REVISION DUE TO AN UNKNOWN REASON. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Insufficient Information
MAUDE report 17949303 ↗InjuryMay 30, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT IS FURTHER REPORTED THAT THE PATIENT WAS REVISED DUE TO SOFT TISSUE IRRITATION OF THE RIGHT TMJ AREA AFTER INITIAL SURGERY. NO INFECTION WAS FOUND. THE IMPLANTS WERE REMOVED AND THEN REPLACED.
Patient problems: Insufficient Information; Skin Inflammation/ Irritation
MAUDE report 17024179 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under P020016. One submission often covers many models, so check the product and lot details in each record.
- Z-0512-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 45mm Rt Stand Off TI Mand Reconstruction of the temporomandibular joint
- Z-0514-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 50mm Lft Stand Off Ti Mand Reconstruction of the temporomandibular joint
- Z-0511-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 45mm Rt Narrow Ti Mand Reconstruction of the temporomandibular joint
- Z-0510-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 45mm Lft Stand Off Ti Mand Reconstruction of the temporomandibular joint
- Z-0516-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 50mm Rt Stand Off Ti Mand Reconstruction of the temporomandibular joint
- Z-0517-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 50mm Rt Standard Ti Mand Reconstruction of the temporomandibular joint
- Z-0515-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 50mm Rt Narrow Ti Mand Reconstruction of the temporomandibular joint
- Z-0522-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 45mm Rt Standard TI Mand Reconstruction of the temporomandibular joint
- Z-0521-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 45mm Lft Standard Ti Mand Reconstruction of the temporomandibular joint
- Z-0518-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 50mm Lft Standard Ti Mandi Reconstruction of the temporomandibular joint
- Z-0509-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 45mm Lft Narrow Ti Mand
- Z-0519-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 55mm Lft Standard Ti Mand Reconstruction of the temporomandibular joint
- Z-0513-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 50mm Lft Narrow Ti Mand Reconstruction of the temporomandibular joint
- Z-0520-2015 · Oct 17, 2014 · TerminatedTotal Temporomandibular Joint Replacement System- 55mm Rt Standard Ti Mand Reconstruction of the temporomandibular joint
- Z-2566-2014 · Sep 20, 2013 · TerminatedBiomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751506 The Total Temporomandibular Joint (TMJ) replacement system is implanted in the jaw to
…and 2 more.
Other Joint, Temporomandibular, Implant devices
- Patient-Fitted TMJ Reconstructive Prosthesis System CHG020TMJ Solutions, Inc. · Joint, Temporomandibular, Implant2 recalls172 reports
- Patient-Fitted TMJ Reconstructive Prosthesis System CHG010TMJ Solutions, Inc. · Joint, Temporomandibular, Implant1 recall94 reports
- TMJ SYSTEM 24-6563Biomet Microfixation, Inc · Joint, Temporomandibular, Implant89 reports
- TMJ SYSTEM 24-6562Biomet Microfixation, Inc · Joint, Temporomandibular, Implant76 reports
- Patient-Fitted TMJ Reconstructive Prosthesis System TYY-NNNNMTMJ Solutions, Inc. · Joint, Temporomandibular, Implant65 reports
- Patient-Fitted TMJ Reconstructive Prosthesis System CHG010AMTMJ Solutions, Inc. · Joint, Temporomandibular, Implant1 recall0 reports
- Patient-Fitted TMJ Reconstructive Prosthesis System TYY-NNNNRMTMJ Solutions, Inc. · Joint, Temporomandibular, Implant38 reports
- Patient-Fitted TMJ Reconstructive Prosthesis System TYY-NNNNLMTMJ Solutions, Inc. · Joint, Temporomandibular, Implant31 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.