Device recall
Z-0715-2022: MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032
FDA device recall · Class II · Stryker Leibinger GmbH & Co. KG
Key facts
| Recall number (Z-number) | Z-0715-2022 |
|---|---|
| Recall event | 89458 |
| Product | MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032 |
| Product code | FTM |
| Recalling firm | Stryker Leibinger GmbH & Co. KG |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 21, 2023 |
| 510(k) numbers | K040364 |
| FEI number | 3002821504 |
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