{
  "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": [
    {
      "country": "United States",
      "city": "Plymouth",
      "address_1": "2905 Northwest Blvd Ste 40",
      "reason_for_recall": "Blue Belt Technologies is conducting a voluntary recall for their Navio PFS system which is used during orthopedic knee surgery. One of the electronic modules inside the computer cart assembly may have a defect in one of its components that could result in a latent failure.",
      "address_2": "",
      "product_quantity": "11",
      "code_info": "SN000090, SN000091, SN000092, SN000187, SN000200, SN000204, SN000226, SN000231, SN000232, SN000246, SN000247",
      "center_classification_date": "20140509",
      "distribution_pattern": "USA: CA, PA, OH, TX.    OUS: BELGIUM, SCOTLAND, UNITED KINGDOM.",
      "state": "MN",
      "product_description": "NavioPFSTM System, Orthopedic Sterotaxic Instrument,  model #'s NPFS-02000, NPFS-02010, NPFS 02020.",
      "report_date": "20140521",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Blue Belt Technologies MN",
      "recall_number": "Z-1575-2014",
      "initial_firm_notification": "Visit",
      "product_type": "Devices",
      "event_id": "68015",
      "termination_date": "20140610",
      "more_code_info": "",
      "recall_initiation_date": "20140411",
      "postal_code": "55441-2673",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}