Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Catalog 314-13-33 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
Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium
Quantity: 40 devices
Why Was This Recalled?
The product may be mislabeled.
Where Was This Sold?
This product was distributed to 21 states: AZ, CA, CO, FL, IL, IN, KY, LA, ME, MD, MN, NV, NY, OH, OK, SC, TN, TX, VA, WA, 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