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Tornier S.A.S. recalls Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement.
Recalled May 14, 2025 · FDA recall Z-1738-2025 · Tornier S.A.S
Hazard
A software bug in Blueprint version 4.2.1 prevents users from accessing cases initiated in previous versions of the software. · FDA Class II
Units
438 users
Sold at
Blueprint Version 4.2.1 is only currently available in the US. Domestic distribution nationwide.
Description
A software bug in Blueprint version 4.2.1 prevents users from accessing cases initiated in previous versions of the software.
Product
Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement.
Manufacturer(s)
Tornier S.A.S.
Made in
France
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →