Device recall
Z-0957-2017: Straumann Drill 1, short, 2.2mm, l 33.0mm, SS-Non sterile. Dental implant…
FDA device recall · Class II · Straumann Manufacturing, Inc.
Key facts
| Recall number (Z-number) | Z-0957-2017 |
|---|---|
| Recall event | 75983 |
| Product | Straumann Drill 1, short, 2.2mm, l 33.0mm, SS-Non sterile. Dental implant accessory Article Number: 044.210 Dental implants drill accessory is intended to prepare osteotomy site for surgical dental implant placement. Dental implants are intended for immediate placement and function on single-tooth… |
| Product code | NDP |
| Recalling firm | Straumann Manufacturing, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 29, 2019 |
| FEI number | 1000121052 |
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