Device recall
Z-0269-2010: Norian CRS Rotary Mixer Cement 10cc sterile
FDA device recall · Class II · Synthes USA (HQ), Inc.
Key facts
| Recall number (Z-number) | Z-0269-2010 |
|---|---|
| Recall event | 53496 |
| Product | Norian CRS Rotary Mixer Cement 10cc sterile |
| Product code | GXP |
| Recalling firm | Synthes USA (HQ), Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 8, 2010 |
| 510(k) numbers | K060445 |
| FEI number | 3005180112 |
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