Device recall
Z-0290-2019: Hoffman LRF Hexapod Strut, Extra Short 131mm-191mm, Model Number 4935-0-030…
FDA device recall · Class II · Stryker GmbH
Key facts
| Recall number (Z-number) | Z-0290-2019 |
|---|---|
| Recall event | 81087 |
| Product | Hoffman LRF Hexapod Strut, Extra Short 131mm-191mm, Model Number 4935-0-030. Product Usage - The Hoffmann LRF System is indicated in pediatric patients and adults for the treatment and fixation of: Open and closed fractures Post-traumatic joint contracture which has resulted in loss of range of… |
| Product code | KTT |
| Recalling firm | Stryker GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 4, 2021 |
| 510(k) numbers | K163656 |
| FEI number | 3002807830 |
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