Drug recall
TMJ Bilateral Implants, REF: CHG020
FDA recall event 98509 · Class II · TMJ Solutions Inc
Key facts
| Event ID | 98509 |
|---|---|
| Recall numbers | Z-2524-2026 |
| Recalling firm | TMJ Solutions Inc |
| Product type | Devices |
| Products | TMJ Bilateral Implants, REF: CHG020 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Feb 11, 2026 |
| Report date | Jul 1, 2026 |
| City | Ventura |
| State | CA |
| Country | United States |
| FEI number | 3001237463 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: