Tornier S.A.S.: Medical Device Recall in 2024 - (Recall #: Z-1883-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Stryker Blueprint Software, Catalog #BPUE001.

Product Classification:

Class II

Date Initiated: April 16, 2024

Date Posted: May 29, 2024

Recall Number: Z-1883-2024

Event ID: 94444

Reason for Recall:

The software bug allows for case planning with anatomic glenoid Perform / Perform Augmented implants and anatomic humeral Tornier Flex implant configurations that are incompatible and do not have regulatory approval.

Status: Ongoing

Product Quantity:

Code Information:

Versions 2.1.4 to 4.0.2, UDI-DI numbers 03700434023114, 03700434023107, 03700434015065, and 03700434015058.

Distribution Pattern:

US Nationwide distribution in the states of FL, KY, NJ, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated