{
  "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": "Ocala",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69422",
      "recalling_firm": "MedX Holdings, Inc.",
      "address_1": "839 Nw 25th Ave",
      "address_2": "N/A",
      "postal_code": "34475-5789",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including MO, IL, ID, and MN and Internationally to Germany and South Korea.",
      "recall_number": "Z-0935-2015",
      "product_description": "Lumbar Extension Machine    for Physical Therapy",
      "product_quantity": "9",
      "reason_for_recall": "Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devices during manufacturing.",
      "recall_initiation_date": "20131203",
      "center_classification_date": "20150107",
      "termination_date": "20160929",
      "report_date": "20150114",
      "code_info": "Serial Numbers: 01531280, 01531279, 01531278, 01531284, 01531283, 01531282, 01531281, 01531288, 01531287",
      "more_code_info": ""
    }
  ]
}