Tornier, Inc: Medical Device Recall in 2023 - (Recall #: Z-0113-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate, 25mm, Offset +3mm, REF DWJ502

Product Classification:

Class II

Date Initiated: September 15, 2023

Date Posted: October 25, 2023

Recall Number: Z-0113-2024

Event ID: 93051

Reason for Recall:

One lot of Tournier Perform Reversed Lateralized Baseplates were found to have been manufactured with 6mm spacers instead of 3mm spacers. This nonconformance prevents the central screw from being able to thread into the baseplate.

Status: Ongoing

Product Quantity: 30 units

Code Information:

UDI/DI 10846832062017, Lot Number 1756123

Distribution Pattern:

US: CA, CO, IL, MA, MN, NC, OR, RI, SC, TN

Voluntary or Mandated:

Voluntary: Firm initiated