Device recall
Z-0219-2015: 10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM…
FDA device recall · Class II · Synthes, Inc.
Key facts
| Recall number (Z-number) | Z-0219-2015 |
|---|---|
| Recall event | 69685 |
| Product | 10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM - Sterile: intended to treat stable and unstable fractures of the proximal femur |
| Product code | HSB |
| Recalling firm | Synthes, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 18, 2015 |
| 510(k) numbers | K011857 |
| FEI number | 3005180112 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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