Device recall
Z-1094-2015: Hemostatic Bone Putty, for use as a water-soluble implant material and for use…
FDA device recall · Class II · Synthes, Inc.
Key facts
| Recall number (Z-number) | Z-1094-2015 |
|---|---|
| Recall event | 70055 |
| Product | Hemostatic Bone Putty, for use as a water-soluble implant material and for use in the control of bleeding from bone surfaces. |
| Product code | MTJ |
| Recalling firm | Synthes, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 30, 2015 |
| 510(k) numbers | K113079 |
| FEI number | 3005180112 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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