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Blue Belt Technologies, Inc

Blue Belt Technologies, Inc Recalls

All product recalls associated with Blue Belt Technologies, Inc.

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

May 2024

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–3 of 3 recalls

CORI Surgical System (Blue Belt) – Marker Registration Error (2024)

CORI Surgical System with Real Intelligence Software exhibits an increased Marker Registration Error (MRE) which may cause tracker arrays to flicker on screen of the CORI Surgical System during use, and may cause surgical delay

FDAMay 7, 2024Nationwide• Blue Belt Technologies, Inc

CORI Robotic Drill (Blue Belt) – Disconnection Errors (2023)

Possibility that the user is unable to resolve drill disconnection error messages.

FDANov 13, 2023Nationwide• Blue Belt Technologies, Inc

CORI RI.KNEE Software (Blue Belt) – Planning Stage Missing (2023)

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

FDASep 7, 2023Nationwide• Blue Belt Technologies, Inc