{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66935",
      "recalling_firm": "Materialise USA LLC",
      "address_1": "44650 Helm Ct",
      "address_2": "N/A",
      "postal_code": "48170-6061",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed in Canada.",
      "recall_number": "Z-0577-2014",
      "product_description": "ProPlan CMF  Guide(s) Model(s)  REF SD900.008 Description: Single Use Only : Patient-Specific Guide,  Orthognathic, Intermediate  Single  Use Only Rx only.      Used as surgical tools to transfer a pre-operative plan to surgery.",
      "product_quantity": "1",
      "reason_for_recall": "Patient Specific Guide contained the incorrect case report.  The case report contains patient specific surgical plan information.",
      "recall_initiation_date": "20131108",
      "center_classification_date": "20131226",
      "termination_date": "20140107",
      "report_date": "20140101",
      "code_info": "Item reference SD900.106; Unique Instrument ID MC13-OVA-OGO_01",
      "more_code_info": ""
    }
  ]
}