{
  "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": "Heverlee",
      "state": "",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70664",
      "recalling_firm": "Materialise N.V.",
      "address_1": "15 Technologielaan",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution to the Netherlands only.",
      "recall_number": "Z-1287-2015",
      "product_description": "Signature TKA GDE/MDL Set 04-05 (Femur & Tibia)    The Signature Patient-Specific Surgical Guides are intended to be used as part of the Signature Personalized Patient Care System. Lt is intended to be used as a guide during the surgical procedure for total and partial knee arthroplasty.",
      "product_quantity": "1 unit",
      "reason_for_recall": "Images belonging to a different patient were used for the production of the patient specific surgical guide.  The incorrect guide may cause a delay in surgery to accommodate the preparation and use of traditional instrumentation.",
      "recall_initiation_date": "20150204",
      "center_classification_date": "20150317",
      "termination_date": "20151030",
      "report_date": "20150325",
      "code_info": "Lot# 124471",
      "more_code_info": ""
    }
  ]
}