FDAApril 10, 2025device

Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

A software bug in Blueprint version 4.2.1 prevents users from accessing cases initiated in previous versions of the software.

What to do

FDA enforcement status: Ongoing

Brands named

tornier s a stornier

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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