Device recall
Z-1035-04: Straumann Dental Implant System SP Profile Drill, Short, 0.35mm, WN, L25.0 mm…
FDA device recall · Class III · The Straumann Company
Key facts
| Recall number (Z-number) | Z-1035-04 |
|---|---|
| Recall event | 29271 |
| Product | Straumann Dental Implant System SP Profile Drill, Short, 0.35mm, WN, L25.0 mm, stainless steel Article No. 044.088 |
| Product code | DZE |
| Recalling firm | The Straumann Company |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 16, 2004 |
| 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