{
  "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": "2026-04-01",
    "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": "86113",
      "recalling_firm": "Materialise N.V.",
      "address_1": "Technologielaan 15",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution to: US including PR and International to UK and  Australia.",
      "recall_number": "Z-2886-2020",
      "product_description": "Match Point System    The Match Point System is intended to by uses as a surgical instrument to assist in the intraoperative positioning of glenoid components used with total and reverse shoulder arthroplasty by referencing anatomic landmarks of the shoulder that are identifiable on preoperative CT-image scans.",
      "product_quantity": "128",
      "reason_for_recall": "The procedure side indicated in the top header of the Shoulder Case Planning Report incorrectly indicated the procedure side as \"Left\" for surgical plans for a \"right\" procedure side.",
      "recall_initiation_date": "20200717",
      "center_classification_date": "20200826",
      "termination_date": "20201223",
      "report_date": "20200902",
      "code_info": "ID #s: 804-03-057, 804-25-148, 804-03-058, 804,07,022    UDI #s: E314804030570, E314804251480, E314804070220"
    }
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}