Device recall
Z-2879-2011: Arthrex Reciprocating Saw Attachment Type: V-600SR Distributed by: Arthrex Inc…
FDA device recall · Class II · W & H DentalWerk Buermoos GMBH
Key facts
| Recall number (Z-number) | Z-2879-2011 |
|---|---|
| Recall event | 59146 |
| Product | Arthrex Reciprocating Saw Attachment Type: V-600SR Distributed by: Arthrex Inc., Naples, Florida United States The system Is a modular electric system, consisting of a handpiece drive, various accessories, and a charging station for machining bones. It can be used in the following areas of… |
| Product code | HWE |
| Recalling firm | W & H DentalWerk Buermoos GMBH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 9, 2015 |
| FEI number | 3003755849 |
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