Device recall
Z-0151-2009: Ray TFC Device with End Caps: Single Patient use; Sterile; Stryker Spine Ray…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-0151-2009 |
|---|---|
| Recall event | 49439 |
| Product | Ray TFC Device with End Caps: Single Patient use; Sterile; Stryker Spine Ray Cage 7-2021 20 (catalog #) mm diameter x 21 mm long. Ray Cages are indicated for use with autogenous bone graft in patients with Degenerative Disc Disease (DDD) at one or two levels for L2 to S1. |
| Product code | MAX |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 4, 2008 |
| PMA numbers | P950019 |
| FEI number | 3004024955 |
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