Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299
FDA Recall Z-0041-2024 · Posted 2023-10-05
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Recalling FirmBlue Belt Technologies, Inc
Recall StatusOpen, Classified
Product CodeOLO
Date Initiated2023-09-07
Product Quantity56 units
Reason for Recall
CORI software was missing a planning stage that appears in cases of significant knee deformation (outside of the range of 3 degrees valgus to 7 degrees varus) when the surgeon chooses to define the femoral rotational reference via the posterior condylar axis
Firm Action
Smith & Nephew, Inc. (Blue Belt Technologies) issued Urgent Medical Device Correction Notice (C-2023-08) on September 7, 2023 via overnight mail. Letter states reason for recall, health risk and action to take:
Required Actions for user/hospital:
1. Complete Correction Notice Acknowledgement Form and submit to [email protected].
2. Prior to use of software, contact your sales representative to update settings.
3. Upon completion of settings update, you may use the CORI Surgical System until the software update is deployed.
4. A Smith & Nephew Robotics Representative will be deployed to your site to implement a new software version to correct the issue once it is available.
Email: [email protected]
Actions for Smith & Nephew Representatives
1. Work with customer to update CORI settings to prevent incorrect configuration.
2. Complete the attached Correction Notice Acknowledgement Form.
3. Upon completion of software upgrade, submit CORI In-Field Service Record to Field Action Team.
Root Cause
Software Design Change
Distribution Pattern
US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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