Device recall
Z-2177-2010: Straumann Impression set for WN solid abutment H 4.00mm POM/ AI. Ref: 040.380…
FDA device recall · Class III · Straumann Manufacturing Inc.
Key facts
| Recall number (Z-number) | Z-2177-2010 |
|---|---|
| Recall event | 56049 |
| Product | Straumann Impression set for WN solid abutment H 4.00mm POM/ AI. Ref : 040.380 Kit Y4021. Intended to aid in the fabrication of dental prosthetics, and be used as a accessory with endosseous dental implants. |
| Product code | NDP |
| Recalling firm | Straumann Manufacturing Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 22, 2011 |
| 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