Device recall
Z-0300-05: Straumann Dental Implant System, SP Profile Drill, Short, 04.2 mm, RN, L25.0 mm…
FDA device recall · Class III · The Straumann Company
Key facts
| Recall number (Z-number) | Z-0300-05 |
|---|---|
| Recall event | 30482 |
| Product | Straumann Dental Implant System, SP Profile Drill, Short, 04.2 mm, RN, L25.0 mm, Stainless steel Ref. Number: 044.084 |
| Product code | NDP |
| Recalling firm | The Straumann Company |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 17, 2005 |
| 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