Device recall
Z-0921-03: Stryker Advanced Cement Mixing System Bowl and 180 Gram Cement Cartridge with…
FDA device recall · Class II · Stryker Instruments, Instruments Div.
Key facts
| Recall number (Z-number) | Z-0921-03 |
|---|---|
| Recall event | 26415 |
| Product | Stryker Advanced Cement Mixing System Bowl and 180 Gram Cement Cartridge with Break-Away Femoral Nozzle for use with Stryker high vacuum cement injection system, 6 pack; part 0306-563-000. |
| Recalling firm | Stryker Instruments, Instruments Div. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 13, 2003 |
| 510(k) numbers | K912190 |
| FEI number | 1811755 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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