{
  "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": "Heverlee",
      "state": "N/A",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72425",
      "recalling_firm": "Materialise N.V.",
      "address_1": "15 Technologielaan",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed in MI, ID, TX, and in France.",
      "recall_number": "Z-0162-2016",
      "product_description": "Signature Patient-Specific Surgical Guides; patient specific instruments used as a guide during surgical procedure for total and partial knee arthroplasty. Part of the Signature Personalized Patient Care System.",
      "product_quantity": "4",
      "reason_for_recall": "Potential inaccuracies in the alignment of the guides.  Surgery was inaccurately planned because the patient image data was incorrectly processed.",
      "recall_initiation_date": "20150923",
      "center_classification_date": "20151023",
      "termination_date": "20160212",
      "report_date": "20151104",
      "code_info": "42422461: Signature SIG CT/TI(A Guides 04-05 Slidex Distal-MP/Premier Tibial & 42422551 : Signature TKA GDE/MDL SET 03-05 MP/Premier Distal- MP/Premier Tibial    42422461  139540  2016-02-17    42-422551  1 391 51  2016-01-14    42422551  1 38805  2016-02-03    42-422551  140787  2016-03-03"
    }
  ]
}