Biomet Microfixation Temporomandibular Joint — Class II medical device recall Z-2566-2014
Terminated recall by Biomet Microfixation, LLC, reported 2014-09-10. Product mix occurred prior to final package and labeling process.
| Recall number | Z-2566-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet Microfixation, LLC, Jacksonville, FL, United States |
| Recall initiated | 2013-09-20 |
| Classified | 2014-09-02 |
| Reported by FDA | 2014-09-10 |
| Terminated | 2014-10-03 |
| Countries outside the US | DK |
| Quantity | 1 |
| Reason classes | labeling |
| Lot numbers | 478490 |
| Model numbers | CP751506 |
Product
Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751506 The Total Temporomandibular Joint (TMJ) replacement system is implanted in the jaw to functionally reconstruct a diseased and/or damaged temporomandibular joint. The Total TMJ replacement system is a two-component system comprised of mandibular condyle and a glenoid fossa components. Both components are available in multiple stock sizes as right and left specific designs and are attached to the bones by screws.
Reason for recall
Product mix occurred prior to final package and labeling process.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2566-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.