{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Heidelberg",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83568",
      "recalling_firm": "Heidelberg Engineering GmbH",
      "address_1": "Tiergartenstr. 15",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide distribution",
      "recall_number": "Z-2437-2019",
      "product_description": "SPECTRALIS with HEYEX2 image management system.   a non-contact ophthalmic diagnostic imaging device.",
      "product_quantity": "29",
      "reason_for_recall": "Error in the default configuration which could lead to the incorrect display of patient master data.",
      "recall_initiation_date": "20190703",
      "center_classification_date": "20190830",
      "termination_date": "20201102",
      "report_date": "20190911",
      "code_info": "All software versions with HEYEX2 image management system    Identification: TFID-3439"
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}