Class II
Medical Device Recall: Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile.
Tornier, Inc · January 3, 2024
Reason for Recall
The incorrect device is contained in the labeled package.
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.
States Affected
AR, AZ, CA, CO, CT, NC, OH, TN, VA
Quantity Affected
50
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0773-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.