Device recall
Z-2839-2016: G1 Dissection Tool - 3mm FLUTED BALL; For cutting and shaping bone including…
FDA device recall · Class II · The Anspach Effort, Inc.
Key facts
| Recall number (Z-number) | Z-2839-2016 |
|---|---|
| Recall event | 75121 |
| Product | G1 Dissection Tool - 3mm FLUTED BALL; For cutting and shaping bone including spine and cranium. |
| Product code | HBE |
| Recalling firm | The Anspach Effort, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 29, 2017 |
| 510(k) numbers | K113476 |
| FEI number | 1045834 |
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