Device recall
Z-0362-2009: ConMed Linvatec Hall Surgical Blades, Sterile INTEX BLADE, Catalog #…
FDA device recall · Class II · Linvatec Corp.
Key facts
| Recall number (Z-number) | Z-0362-2009 |
|---|---|
| Recall event | 47848 |
| Product | ConMed Linvatec Hall Surgical Blades, Sterile INTEX BLADE, Catalog # 00507132000, 00507134000, 00507135300, 00507135400, 00507135600, 00507130000, 00507130300, 00507130400, 00507130500, 00507131400, 00507133000, 00507133300, 00507133400, 00507132300, 00507132400, 00507132500, and 00507132600. ConMed… |
| 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