Class III — Integra LifeSciences Corp.
| Recalling firm | Integra LifeSciences Corporation |
|---|---|
| Registered facility | View this company's 15 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | The firm received one complaint from one non-US sales representative (France) that the label on the UNI-CP plate was incorrect. |
| Product | The UNI-CP System; Model Number: 330230SND. |
| Quantity | 39 units |
| Distribution | Nationwide |
| Initiated | 2017-01-25 |
| Classified | 2017-03-04 |
| Terminated | 2017-11-08 |
| Recall number | Z-1410-2017 |
| 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 III recall — Integra LifeSciences Corp. (Z-1410-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/76408/
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