Device recall
Z-1965-2017: 16CM MIN INVASIVE ATTACH, BLACK MAX
FDA device recall · Class II · The Anspach Effort, Inc.
Key facts
| Recall number (Z-number) | Z-1965-2017 |
|---|---|
| Recall event | 76059 |
| Product | 16CM MIN INVASIVE ATTACH, BLACK MAX |
| Product code | BWN |
| Recalling firm | The Anspach Effort, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 26, 2019 |
| 510(k) numbers | K955084 |
| FEI number | 1045834 |
At a glance
- 1–9 Linked 510(k)s
- 100–999 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