{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Plymouth",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90704",
      "recalling_firm": "Materialise USA LLC",
      "address_1": "44650 Helm Ct",
      "address_2": "",
      "postal_code": "48170-6061",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the state of MD.",
      "recall_number": "Z-1569-2022",
      "product_description": "ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear  Identification number SD900.208",
      "product_quantity": "1 unit",
      "reason_for_recall": "MU22-INA-DUQ case was labeled as MU22-INA-DUQ but  was shipped with the Anatomical Model of case MU22-NOF-SAK",
      "recall_initiation_date": "20220713",
      "center_classification_date": "20220824",
      "report_date": "20220831",
      "code_info": "Unique Device Identifier (01)05420060352089(10)MU22INADUQ Lot Number: MU22-INQ-DUQ",
      "more_code_info": ""
    }
  ]
}