Tornier S.A.S.: Medical Device Recall in 2025 - (Recall #: Z-1738-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 10, 2025

Date Posted: May 14, 2025

Recall Number: Z-1738-2025

Event ID: 96651

Reason for Recall:

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

Status: Ongoing

Product Quantity: 438 users

Code Information:

Software Version 4.2.1

Distribution Pattern:

Blueprint Version 4.2.1 is only currently available in the US. Domestic distribution nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated