Device recall
Z-0168-2020: Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the…
FDA device recall · Class II · Exactech, Inc.
Key facts
| Recall number (Z-number) | Z-0168-2020 |
|---|---|
| Recall event | 83855 |
| Product | Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the implantation of Equinoxe Shoulder System components according to a conventional technique for total shoulder replacement. The wire is single-use, provided sterile, and intended for transient use. |
| Product code | LRN |
| Recalling firm | Exactech, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2023 |
| FEI number | 1038671 |
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