Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a Recalled by Advanced Orthogonal Equipment, Incorporated Due to Unapproved medical device
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 Advanced Orthogonal Equipment, Incorporated directly.
Affected Products
Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making Chiropractic adjustments to the Atlas vertebra.
Quantity: 54
Why Was This Recalled?
Unapproved medical device
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Advanced Orthogonal Equipment, Incorporated
Advanced Orthogonal Equipment, Incorporated has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report