PlainRecalls
FDA Devices Moderate Class II Ongoing

Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile.

Reported: January 31, 2024 Initiated: January 3, 2024 #Z-0773-2024

Product Description

Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile.

Reason for Recall

The incorrect device is contained in the labeled package.

Details

Recalling Firm
Tornier, Inc
Units Affected
50
Distribution
Distribution was made to AR, AZ, CA, CO, CT, NC, OH, TN, and VA. There was no military/government distribution. Foreign distribution was made to Australia, France, and Italy.
Location
Bloomington, MN

Frequently Asked Questions

What product was recalled?
Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile.. Recalled by Tornier, Inc. Units affected: 50.
Why was this product recalled?
The incorrect device is contained in the labeled package.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 31, 2024. Severity: Moderate. Recall number: Z-0773-2024.