Device recall
Z-1783-2012: Accessories for the Captiva Spine FuseLOX Lumbar Cage. Products are labeled in…
FDA device recall · Class II · Captiva Spine, Inc
Key facts
| Recall number (Z-number) | Z-1783-2012 |
|---|---|
| Recall event | 61925 |
| Product | Accessories for the Captiva Spine FuseLOX Lumbar Cage. Products are labeled in part: "FuseLOX Lumbar Cage Lumbar Interbody Fusion Device***Description:***Part Number:***Lot Number:***Quantity: 1***Material: PEEK-OPTIMA LT1, Tantalum ASTM F560***Non-Sterile-Single Use Only (See package insert for… |
| Product code | MAX |
| Recalling firm | Captiva Spine, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 24, 2013 |
| FEI number | 3006082533 |
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