Device recall
Z-1856-2025: Glidewell HT Implant Twist Drill 1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code…
FDA device recall · Class II · Prismatik Dentalcraft, Inc.
Key facts
| Recall number (Z-number) | Z-1856-2025 |
|---|---|
| Recall event | 96711 |
| Product | Glidewell HT Implant Twist Drill 1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code: +D7457071SRG02660/$$76254798/16D20250219V The Glidewell HT" Implant Twist Drill is indicated to prepare the site for placement of endosseous dental implants when tissue contact will last less than 1 hour. The Glidewell HT"… |
| Product code | NDP |
| Recalling firm | Prismatik Dentalcraft, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3011649314 |
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