FDA Device recall Z-0708-2024
CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S
- FDA Device
- Class II
- ongoing
- Published 2024-01-17
On 2024-01-17 the FDA classified a Class II recall of CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S by Blue Belt Technologies, citing possibility that the user is unable to resolve drill disconnection error messages.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0708-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-11-13 |
| Published | 2024-01-17 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Blue Belt Technologies |
| Distribution | US |
Product
CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S
Reason
Possibility that the user is unable to resolve drill disconnection error messages.
Identifiers
| code_info | UDI-DI: 00885556757321 and 00885556780886; Serial No. SN00001 through SN001202, SN500001 through SN502583. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0708-2024%22
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