Device recall
Z-2172-2025: The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to…
FDA device recall · Class II · Implant Direct Sybron Manufacturing LLC
Key facts
| Recall number (Z-number) | Z-2172-2025 |
|---|---|
| Recall event | 96778 |
| Product | The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop length, and facilitate the mounting/removal of the Drill Stops. The Drill Stop Kit includes the Release Bracket, which is used for mounting and removing Drill Stops, as well as… |
| Product code | KCT |
| Recalling firm | Implant Direct Sybron Manufacturing LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K200858 |
| FEI number | 3001617766 |
At a glance
- 1–9 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