Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Verasense Knee System Recalled by Orthosensor, Inc. Due to Presence of one inoperable (dead) sensor pad.
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 Orthosensor, Inc. directly.
Affected Products
Verasense Knee System, Model SYK-TRCR 02. Intelligent disposable tibial insert that measures dynamic loads during orthopedic knee surgery.
Quantity: 22 devices
Why Was This Recalled?
Presence of one inoperable (dead) sensor pad.
Where Was This Sold?
This product was distributed to 6 states: CA, IL, MI, NV, NY, VA
About Orthosensor, Inc.
Orthosensor, Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report