Device recall
Z-1457-2014: The Synthes Hohmann Retractor, 43 mm Long Shank, Angled 235 mm Product Usage…
FDA device recall · Class II · Synthes, Inc.
Key facts
| Recall number (Z-number) | Z-1457-2014 |
|---|---|
| Recall event | 67560 |
| Product | The Synthes Hohmann Retractor, 43 mm Long Shank, Angled 235 mm Product Usage: Used to expose bone for procedures. |
| Product code | GAD |
| Recalling firm | Synthes, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 10, 2015 |
| FEI number | 3005180112 |
At a glance
- None 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