Device recall
Z-0336-2008: Axya Anchor, 5.0 mm Titanium in Super Kit, Catalog Number: CAT1270, Axya…
FDA device recall · Class II · Axya Medical
Key facts
| Recall number (Z-number) | Z-0336-2008 |
|---|---|
| Recall event | 44963 |
| Product | Axya Anchor, 5.0 mm Titanium in Super Kit, Catalog Number: CAT1270, Axya Medical, Inc., Beverly, MA 01915 |
| Product code | MBI |
| Recalling firm | Axya Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2012 |
| FEI number | 3000718467 |
At a glance
- None 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