Device recall
Z-1008-2024: Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023, REF 001156T0), carbide…
FDA device recall · Class II · Brasseler USA I Lp
Key facts
| Recall number (Z-number) | Z-1008-2024 |
|---|---|
| Recall event | 93809 |
| Product | Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023, REF 001156T0), carbide dental bur, 10 burs/package, Rx. |
| Product code | EJL |
| Recalling firm | Brasseler USA I Lp |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1032227 |
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