Device recall
Z-0949-2008: Kyphon, Functional Anaesthetic Discography (F.A.D.) Introducer Needle, Catalog…
FDA device recall · Class II · Kyphon Inc
Key facts
| Recall number (Z-number) | Z-0949-2008 |
|---|---|
| Recall event | 39366 |
| Product | Kyphon, Functional Anaesthetic Discography (F.A.D.) Introducer Needle, Catalog Number: D01B, Kyphon, Inc., Sunnyvale, Ca 94089 |
| Product code | BSP |
| Recalling firm | Kyphon Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 10, 2008 |
| FEI number | 3004904811 |
At a glance
- None Linked 510(k)s
- 1–9 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