TMJ Bilateral Implants — Class II medical device recall Z-2524-2026
Ongoing recall by TMJ Solutions Inc, reported 2026-07-01, distributed nationwide. Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a
| Recall number | Z-2524-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | TMJ Solutions Inc, Ventura, CA, United States |
| Recall initiated | 2026-02-11 |
| Classified | 2026-06-22 |
| Reported by FDA | 2026-07-01 |
| Distributed | Nationwide (US) |
| Quantity | 1 |
| UPC / GTIN / UDI-DI | 07613327626575 |
| Lot numbers | 2508181038 |
| Model numbers | CHG020 |
Product
TMJ Bilateral Implants, REF: CHG020
Reason for recall
Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.
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-2524-2026. 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.