Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4 — Class II medical device recall Z-0751-2025
Ongoing recall by SEASPINE ORTHOPEDICS CORPORATION, reported 2025-01-01, distributed nationwide. Due to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
| Recall number | Z-0751-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | SEASPINE ORTHOPEDICS CORPORATION, Carlsbad, CA, United States |
| Recall initiated | 2024-10-29 |
| Classified | 2024-12-23 |
| Reported by FDA | 2025-01-01 |
| Distributed | Nationwide (US) |
| Quantity | 92 devices |
| UPC / GTIN / UDI-DI | 10889981185640 |
| Lot numbers | 79-0002, MM1002742E, MM1003065E |
| Model numbers | 79-0002 |
Product
Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm, Small Stature, T25, BT Model/Catalog Number: 79-0002 Software Version: N/A Product Description: Locking Cap Component: No
Reason for recall
Due to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
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-0751-2025. 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.