{
  "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": "2026-04-15",
    "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": "Ortho Kinematics notified customers that errors were contained in Radiological Read Report and VMA Report for the VMA test. The error resulted from an administrative error of VMA user account settings and has been fixed.",
      "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), 2.3.239 - 2.3.254.    Product Usage:  VMA software is a quantitative imaging software application intended to be used to process digital image files.",
      "report_date": "20180829",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ortho Kinematics, Inc",
      "recall_number": "Z-2891-2018",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "80771",
      "more_code_info": "",
      "recall_initiation_date": "20170302",
      "postal_code": "78746-3352",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}