Device recall
Z-1526-2018: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of…
FDA device recall · Class II · Stryker GmbH
Key facts
| Recall number (Z-number) | Z-1526-2018 |
|---|---|
| Recall event | 79751 |
| Product | Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity correction, bone and soft tissue reconstruction in pediatric patients and adults. |
| Product code | KTT |
| Recalling firm | Stryker GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 21, 2020 |
| 510(k) numbers | K113327 |
| 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