Device recall
Z-1479-2008: Sequoia Spinal System Surgical Kits; Pedicle screw spinal system; Non-sterile…
FDA device recall · Class II · Abbott Spine
Key facts
| Recall number (Z-number) | Z-1479-2008 |
|---|---|
| Recall event | 46888 |
| Product | Sequoia Spinal System Surgical Kits; Pedicle screw spinal system; Non-sterile (kits intended to be sterilized prior to use); Rx Only; The Sequoia Spinal System is designed to aid in the surgical correction of several types of spinal conditions. The product is a system of smaller devices used to… |
| Product code | NKB |
| Recalling firm | Abbott Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 28, 2008 |
| 510(k) numbers | K072672 |
| FEI number | 3000718496 |
At a glance
- 1–9 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