Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Altiva / Exactech Spine Recalled by Exactech, Inc. Due to Incorrect thread form on the screw.
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
Altiva / Exactech Spine, Large Set Screw, Catalog Number 28202, Lot Number AS05107. Intended to provide immobilization and stabilization of spinal segments.
Quantity: 749 devices
Why Was This Recalled?
Incorrect thread form on the screw.
Where Was This Sold?
This product was distributed to 6 states: FL, GA, IL, NY, TX, WA
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