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Advanced Orthogonal Equipment, Incorporated recalls Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making
Recalled July 31, 2013 · FDA recall Z-1809-2013 · Advanced Orthogonal Equipment, Incorporated
Hazard
Unapproved medical device · FDA Class II
Units
54
Sold at
Nationwide distribution: US including states of: AL, CA, CO, FL, GA, ID, KY, MD, NC, NJ, NY, OH, PA, TN, VA, and WA.
Description
Unapproved medical device
Product
Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making Chiropractic adjustments to the Atlas vertebra.
Manufacturer(s)
Advanced Orthogonal Equipment, Incorporated
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →