Class II — Captiva Spine, Inc
| Recalling firm | CAPTIVA SPINE |
|---|---|
| Registered facility | CAPTIVA SPINE, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | It is possible for the titanium color-coded ring to detach from the Reamers. |
| Product | Captiva's lumbar intervertebral fusion system Reamers (color code rings on the Reamers). |
| Quantity | 233 devices |
| Distribution | GA, IN, FL, UT, AZ, CA, and NY |
| Initiated | 2015-02-25 |
| Classified | 2015-04-21 |
| Terminated | 2015-06-01 |
| Recall number | Z-1480-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Captiva Spine, Inc (Z-1480-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/70710/
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