{
  "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": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74213",
      "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": "One consignee, Indiana.",
      "recall_number": "Z-1941-2016",
      "product_description": "Signature TKA GDE/MDL Set 04-05    Patient-specific surgical guide and instrument set.",
      "product_quantity": "1",
      "reason_for_recall": "A patient specific case of Signature Personalized Patient Care System Knee Guides included a femur guide which does not match the patient associated with the case.  If the issue is not identified prior to surgery, the personalized patient specific guide would provide an improper fit and would not be able to be used.",
      "recall_initiation_date": "20160503",
      "center_classification_date": "20160609",
      "termination_date": "20160628",
      "report_date": "20160615",
      "code_info": "Lot #154970"
    }
  ]
}