Device recall
Z-1876-2008: Straumann Handpiece Driver for RN Solid Abutment 6 L 26.0mm,Stainless Steel…
FDA device recall · Class III · Straumann Manufacturing Inc.
Key facts
| Recall number (Z-number) | Z-1876-2008 |
|---|---|
| Recall event | 48610 |
| Product | Straumann Handpiece Driver for RN Solid Abutment 6 L 26.0mm,Stainless Steel -- Reference Number: 80426. Product is intended as radiographic guides and surgical templates for the initial placement of the 2.2 mm pilot drill used in the site preparation for the placement of Straumann dental implants. |
| Product code | DZE |
| Recalling firm | Straumann Manufacturing Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 6, 2009 |
| FEI number | 1000121052 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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