Device recall
Z-3184-2011: Straumann coDiagnostiX, version 8.0, used to guide a clinician in the proper…
FDA device recall · Class II · Straumann Manufacturing Inc.
Key facts
| Recall number (Z-number) | Z-3184-2011 |
|---|---|
| Recall event | 59797 |
| Product | Straumann coDiagnostiX, version 8.0, used to guide a clinician in the proper implant selection, oral placement and the proper selection of an oral drill. Imaging processing System |
| Product code | LLZ |
| Recalling firm | Straumann Manufacturing Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2012 |
| 510(k) numbers | K071636 |
| FEI number | 1000121052 |
At a glance
- 1–9 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