Tornier, Inc: Medical Device Recall in 2024 - (Recall #: Z-3309-2024)

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 Tornier Perform Humeral System, Reversed Insert, 45%, REF DWP2393, for shoulder arthroplasty

Product Classification:

Class II

Date Initiated: August 29, 2024

Date Posted: October 9, 2024

Recall Number: Z-3309-2024

Event ID: 95245

Reason for Recall:

Devices from one lot of Perform" Reversed Inserts may contain a locking ring that was assembled upside down which would prevent the humeral insert from securely seating in the stem or spacer.

Status: Ongoing

Product Quantity: 38 units

Code Information:

GTIN 00846832084494, Batch Lot # 1495AY

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated