Device recall
Z-1958-2010: Stryker 8 MM AVS TL Trial Spacer; Catalog number: 48389408. Manufactured by…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-1958-2010 |
|---|---|
| Recall event | 55710 |
| Product | Stryker 8 MM AVS TL Trial Spacer; Catalog number: 48389408. Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ 07401. Intended for use in the thoraco-lumbar spine. |
| Product code | MDM |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 6, 2012 |
| FEI number | 3004024955 |
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