CLASS II ONGOING Device recall · Reported 17 Jan 2024 · FDA Enforcement Report
Cori Real Intelligence Robotic Drill recalled by Blue Belt Technologies
Blue Belt Technologies is recalling Cori Real Intelligence Robotic Drill, Product No. ROB10013 and ROB10013S, distributed nationwide in the US. The recall was initiated on 13 Nov 2023 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0708-2024
- FDA event ID
- 93620
- Recalling firm
- Blue Belt Technologies, Pittsburgh, PA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 13 Nov 2023
- FDA classified
- 11 Jan 2024
- Reported
- 17 Jan 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 13 Nov 2023 | Recall initiated by company | |
| 11 Jan 2024 | Classified by FDA | +59 days |
| 17 Jan 2024 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Possibility that the user is unable to resolve drill disconnection error messages.
Product as listed by the FDA
CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S
Where it was distributed
Domestic: Nationwide Distribution.
Questions about this recall
Is Cori Real Intelligence Robotic Drill, Product No. ROB10013 and ROB10013S recalled?
Yes. Blue Belt Technologies recalled Cori Real Intelligence Robotic Drill, Product No. ROB10013 and ROB10013S on 13 Nov 2023. The recall is Class II and its status is Ongoing. Recall number Z-0708-2024.
Why was it recalled?
Possibility that the user is unable to resolve drill disconnection error messages.
Which lots are affected?
UDI-DI: 00885556757321 and 00885556780886; Serial No. SN00001 through SN001202, SN500001 through SN502583.
Where was it sold?
Domestic: Nationwide Distribution.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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