{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Minnetonka",
      "address_1": "5101 Shady Oak Rd S",
      "reason_for_recall": "Breaking of the HFD200 Drive Knob force indicator due to over-torqueing of the drive knob beyond the maximum allowable pinning force specification may result in the clinical staff unknowingly pinning the patient's skull with insufficient force; the clinical staff unknowingly pinning the patient's skull with excessive force; or the clinical staff identifying the issue and not being able to continue with the procedure.",
      "address_2": "",
      "product_quantity": "3 units",
      "code_info": "HFD Serial Number  Drive Knob Serial Number   10002481  10003305  10002351  10005723  10004247  10002448",
      "center_classification_date": "20191018",
      "distribution_pattern": "TN, NH, FL",
      "state": "MN",
      "product_description": "IMRIS MR/X-ray head fixation device, Model HFD200",
      "report_date": "20191030",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Deerfield Imaging, Inc.",
      "recall_number": "Z-0163-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83278",
      "termination_date": "20201029",
      "more_code_info": "",
      "recall_initiation_date": "20190626",
      "postal_code": "55343-4100",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}