Reported Jul 31, 2013 · Terminated

Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making…

Advanced Orthogonal Equipment, Incorporated

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Advanced Orthogonal Equipment, Incorporated · 2201 62nd Ave N · Saint Petersburg, FL · 33702-5660

Is this the product you have?

  • Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making Chiropractic adjustments to the Atlas vertebra.
Lot codes and dates
  • Serial numbers
    • 001
    • 002
    • 008
    • 007
    • 006
    • 0010
    • 009
    • 011
    • 016
    • 015
    • 014
    • 023
    • 017
    • 018
    • 019
    • 020
    • 021
    • 024
    • 025
    • 022
    • 027
    • 026
    • 028
    • 029
    • 030
    • 031
    • 032
    • 033
    • 034
    • 035
    • 036
    • 038
    • 039
    • 037
    • 041
    • 042
    • 040
    • 043
    • 044
    • 045
    • 046
    • 048
    • 049
    • 050
    • 052
    • 053
    • 055
    • 056
    • 060
    • 058
    • 059
    • and 061
Amount recalled
54

Where it was sold

Why it was recalled

Unapproved medical device

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 25, 2019 · Data as of Sep 19, 6:14 PM UTC

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