Device recall
Z-2418-2019: Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 The EPF system is designed…
FDA device recall · Class II · Stryker GmbH
Key facts
| Recall number (Z-number) | Z-2418-2019 |
|---|---|
| Recall event | 83423 |
| Product | Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus. |
| Product code | HRX |
| Recalling firm | Stryker GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 24, 2020 |
| 510(k) numbers | K940230 |
| FEI number | 3002807830 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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