FDA Device recall Z-1410-2017
The UNI-CP System
- FDA Device
- Class III
- terminated
- Published 2017-03-15
On 2017-03-15 the FDA classified a Class III recall of The UNI-CP System by Integra Lifesciences, citing the firm received one complaint from one non-US sales representative (France) that the label on the UNI-CP plate was incorrect.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1410-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-01-25 |
| Published | 2017-03-15 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Integra Lifesciences |
| Distribution | US |
Product
The UNI-CP System; Model Number: 330230SND.
Reason
The firm received one complaint from one non-US sales representative (France) that the label on the UNI-CP plate was incorrect.
Identifiers
| code_info | Lot # FEDT |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1410-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.