Device recall
Z-2390-2021: Norton Arm Kit, Product Code 711400, (previous product code 031001), Sample Kit…
FDA device recall · Class II · Aspen Surgical Products, Inc.
Key facts
| Recall number (Z-number) | Z-2390-2021 |
|---|---|
| Recall event | 88476 |
| Product | Norton Arm Kit, Product Code 711400, (previous product code 031001), Sample Kit S711400 |
| Product code | CCX |
| Recalling firm | Aspen Surgical Products, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 26, 2022 |
| FEI number | 3002750084 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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