CORI REAL INTELLIGENCE Robotic Drill — Class II medical device recall Z-0708-2024
Ongoing recall by Blue Belt Technologies, Inc, reported 2024-01-17, distributed nationwide. Possibility that the user is unable to resolve drill disconnection error messages.
| Recall number | Z-0708-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Blue Belt Technologies, Inc, Pittsburgh, PA, United States |
| Recall initiated | 2023-11-13 |
| Classified | 2024-01-11 |
| Reported by FDA | 2024-01-17 |
| Distributed | Nationwide (US) |
| Quantity | 1,859 units |
| UPC / GTIN / UDI-DI | 00885556757321, 00885556780886 |
| Serial numbers | SN00001 |
Product
CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S
Reason for recall
Possibility that the user is unable to resolve drill disconnection error messages.
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-0708-2024. 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.