Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Equinoxe Cage Recalled by Exactech, Inc. Due to Mislabeling
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Exactech, Inc. directly.
Affected Products
Equinoxe Cage, Glenoid, Alpha, Medium Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally mature individuals with degenerative diseases or fractures of the glenohumeral joint where total or hemi- arthroplasty is determined by the surgeon to be the preferred method of treatment.
Quantity: 30
Why Was This Recalled?
Potentially mislabeled.
Where Was This Sold?
This product was distributed to 14 states: AL, AZ, CA, CO, FL, GA, ME, MN, OH, OK, SC, TN, VA, WI
About Exactech, Inc.
Exactech, Inc. has 211 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report