Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Surgical Equipment

Blue Belt Technologies, Inc: CORI Robotic Drill Recalled Due to Drill Disconnection Error Messages

Agency Publication Date: January 11, 2024
Share:
Sign in to monitor this recall

Summary

Blue Belt Technologies, Inc. has recalled approximately 1,859 units of the CORI REAL INTELLIGENCE Robotic Drill due to a potential software or hardware issue where users may be unable to resolve drill disconnection error messages. This issue affects units with product numbers ROB10013 and ROB10013S sold nationwide. If this error occurs during a surgical procedure and cannot be resolved, it may lead to delays or the inability to complete the robotic portion of the surgery. Consumers should contact the manufacturer immediately to understand the necessary steps for their specific device.

Risk

If a drill disconnection error message persists and cannot be cleared by the user, the robotic drill may become unusable during a medical procedure, potentially leading to surgical delays or a transition to manual surgical techniques.

What You Should Do

  1. Check your device for Product Numbers ROB10013 or ROB10013S and verify if the Serial Number falls within the affected ranges: SN00001 through SN001202 or SN500001 through SN502583.
  2. Verify the UDI-DI on the device labeling matches either 00885556757321 or 00885556780886.
  3. Contact your healthcare provider or Blue Belt Technologies, Inc. at their Pittsburgh headquarters for specific instructions regarding software updates or hardware inspections to resolve the disconnection errors.
  4. Report any incidents of persistent disconnection errors to the manufacturer and through the FDA's MedWatch reporting program.
  5. For further information or questions about this recall, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer guidance following firm-initiated notification letter

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: CORI REAL INTELLIGENCE Robotic Drill (Product No. ROB10013)
Model / REF:
ROB10013
UPC Codes:
00885556757321
Lot Numbers:
Serial No. SN00001 through SN001202
Serial No. SN500001 through SN502583
Product: CORI REAL INTELLIGENCE Robotic Drill (Product No. ROB10013S)
Model / REF:
ROB10013S
UPC Codes:
00885556780886
Lot Numbers:
Serial No. SN00001 through SN001202
Serial No. SN500001 through SN502583

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93620
Status: Active
Manufacturer: Blue Belt Technologies, Inc
Sold By: Direct distribution
Manufactured In: United States
Units Affected: 1859 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.