Device recall
Z-0394-2009: ConMed Linvatec Hall Surgical Blades, Sterile ST REPL STRYKER SAG, Catalog #…
FDA device recall · Class II · Linvatec Corp.
Key facts
| Recall number (Z-number) | Z-0394-2009 |
|---|---|
| Recall event | 47848 |
| Product | ConMed Linvatec Hall Surgical Blades, Sterile ST REPL STRYKER SAG, Catalog # 00507215200, 00507215800, 00507215000, 00507210900, 00507210500, 00507211100, 00507215100, 00507210200, 00507210000 00507218300, and 00507214000. ConMed Linvatec Hall (R) Surgical Blades are intended for use in small bone… |
| Product code | GET |
| Recalling firm | Linvatec Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 15, 2009 |
| FEI number | 1017294 |
At a glance
- None Linked 510(k)s
- 10–99 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