{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "West Lake Hills",
      "address_1": "110 Wild Basin Rd Ste 250",
      "reason_for_recall": "This email is to provide notification that, due to a software bug that has been corrected, the Radiological Read Report for the VMA test(s) contained an error.",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "00868579000209",
      "center_classification_date": "20180822",
      "distribution_pattern": "U.S. Nationwide Distribution",
      "state": "TX",
      "product_description": "Vertebral Motion Analyzer (VMA), 2.3.250.    Product System, image processing, radiological",
      "report_date": "20180829",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ortho Kinematics, Inc",
      "recall_number": "Z-2889-2018",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "80769",
      "more_code_info": "",
      "recall_initiation_date": "20180523",
      "postal_code": "78746-3352",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}