The UNI-CP System — Class III medical device recall Z-1410-2017
Terminated recall by Integra LifeSciences Corp., reported 2017-03-15, distributed nationwide. The firm received one complaint from one non-US sales representative (France) that the label on the UNI-CP pla
| Recall number | Z-1410-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Integra LifeSciences Corp., Plainsboro, NJ, United States |
| Recall initiated | 2017-01-25 |
| Classified | 2017-03-04 |
| Reported by FDA | 2017-03-15 |
| Terminated | 2017-11-08 |
| Distributed | Nationwide (US) |
| Quantity | 39 units |
| Reason classes | labeling |
| Model numbers | 330230SND |
Product
The UNI-CP System; Model Number: 330230SND.
Reason for recall
The firm received one complaint from one non-US sales representative (France) that the label on the UNI-CP plate was incorrect.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1410-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.