Device recall
Z-1034-2008: Stryker Instruments Minor modification product, 550-19-20 with 304.8mm length…
FDA device recall · Class II · Stryker Instruments Div. of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-1034-2008 |
|---|---|
| Recall event | 46341 |
| Product | Stryker Instruments Minor modification product, 550-19-20 with 304.8mm length, sterile, product of Ireland, Stryker Instruments, Kalamazoo, MI; REF 5500019020S3. |
| Product code | HBE |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 1, 2009 |
| 510(k) numbers | K032303 |
| FEI number | 1811755 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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