{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Petersburg",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65391",
      "recalling_firm": "Advanced Orthogonal Equipment, Incorporated",
      "address_1": "2201 62nd Ave N",
      "address_2": "N/A",
      "postal_code": "33702-5660",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution: US including states of:  AL, CA, CO, FL, GA, ID, KY, MD, NC, NJ, NY, OH, PA, TN, VA, and WA.",
      "recall_number": "Z-1809-2013",
      "product_description": "Advanced Orthogonal Percussion Adjusting Instrument     Indicated for use by a licensed Chiropractor to assist in making Chiropractic adjustments to the Atlas vertebra.",
      "product_quantity": "54",
      "reason_for_recall": "Unapproved medical device",
      "recall_initiation_date": "20130306",
      "center_classification_date": "20130725",
      "termination_date": "20191125",
      "report_date": "20130731",
      "code_info": "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",
      "more_code_info": ""
    }
  ]
}