Device recall
Z-0780-2020: Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN…
FDA device recall · Class II · Stryker GmbH
Key facts
| Recall number (Z-number) | Z-0780-2020 |
|---|---|
| Recall event | 84458 |
| Product | Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertion and withdrawal of nails through the Targeting Device Catalog Number: 2351-0050 |
| Product code | HRS |
| Recalling firm | Stryker GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 9, 2020 |
| FEI number | 3002807830 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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