Device recall
Z-0488-2026: TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
FDA device recall · Class I · TMJ Solutions Inc
Key facts
| Recall number (Z-number) | Z-0488-2026 |
|---|---|
| Recall event | 97703 |
| Product | TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only |
| Product code | LZD |
| Recalling firm | TMJ Solutions Inc |
| Recall class | Class I |
| Status | Open, Classified |
| PMA numbers | P980052 |
| FEI number | 3001237463 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database