Device recall
Z-2105-2023: Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020…
FDA device recall · Class II · Wright Medical Technology, Inc.
Key facts
| Recall number (Z-number) | Z-2105-2023 |
|---|---|
| Recall event | 92460 |
| Product | Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile. |
| Product code | HSN |
| Recalling firm | Wright Medical Technology, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K123954 |
| FEI number | 3010667733 |
At a glance
- 1–9 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