Device recall
Z-1676-2021: Rubber Dam Clamp, KSK - Product Usage: used for prevention of contamination by…
FDA device recall · Class II · Dentech Corp.
Key facts
| Recall number (Z-number) | Z-1676-2021 |
|---|---|
| Recall event | 87847 |
| Product | Rubber Dam Clamp, KSK - Product Usage: used for prevention of contamination by saliva and moisture prevention during dental treatment. |
| Product code | EEF |
| Recalling firm | Dentech Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 12, 2023 |
| FEI number | 3002809535 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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