{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Heiligenhaus",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76362",
      "recalling_firm": "Hidrex GmbH",
      "address_1": "Otto-Hahn-Str. 12",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide throughout the US",
      "recall_number": "Z-1237-2017",
      "product_description": "Hidrex USA DVP1000",
      "product_quantity": "180 units",
      "reason_for_recall": "The device was reclassified from a class III device to a class II device and there are new documentation requirements.",
      "recall_initiation_date": "20170130",
      "center_classification_date": "20170222",
      "termination_date": "20170804",
      "report_date": "20170301",
      "code_info": "SN# 16-3.6190 to 16-3.6319, 17-3.6001 to  17-3.6050"
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}