The Recall Desk

Manufacturer

Advanced Orthogonal Equipment, Incorporated

1 recall in our database name Advanced Orthogonal Equipment, Incorporated as the manufacturing or recalling firm.

What the numbers show

Total
1
Critical
0
Severe
0
Most recent
2013-07-31

Of the 1 recalls from Advanced Orthogonal Equipment, Incorporated we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–1 of 1

  • ModerateFDA (Devices)·Z-1809-2013·2013-07-31

    FDA Recalls Unapproved Advanced Orthogonal Percussion Adjusting Instruments

    The FDA is recalling 54 Advanced Orthogonal Percussion Adjusting Instruments because they are unapproved medical devices. The recall covers units distributed nationwide to chiropractors.

    Product
    Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making Chiropractic adjustments to the Atlas vertebra.
    Category
    Medical Device
    Distribution
    Distributed nationwide