Tornier, Inc: Medical Device Recall in 2026 - (Recall #: Z-1237-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE, catalog number DWJ318

Product Classification:

Class II

Date Initiated: December 19, 2025

Date Posted: February 11, 2026

Recall Number: Z-1237-2026

Event ID: 98123

Reason for Recall:

A specific lot of screws is incorrectly labeled. Screws are labeled as 5.0mmx18mm but actual screws are 5.00mmx14mm. If mismatch is detected during surgery, the issue may cause a minor delay in surgery. If not detected and incorrect screw is used, issue may increase risk of earlier mechanical failure, loosening, and need for revision surgery.

Status: Ongoing

Product Quantity: 427

Code Information:

Lot AZ4824290

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated