{
  "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": "Teltow",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78349",
      "recalling_firm": "Somatex Medical Technologies GmbH",
      "address_1": "Rheinstr. 7 d",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NY - Only one US distributor",
      "recall_number": "Z-0410-2018",
      "product_description": "TUMARK Q, Length 12 cm, Diameter 18G, GTIN 04250195603081, REF 271500, STERILE",
      "product_quantity": "N/A",
      "reason_for_recall": "There is a potential risk of puncture to the packaging material which can compromise the devices sterility, making it non-sterile.",
      "recall_initiation_date": "20170522",
      "center_classification_date": "20180124",
      "termination_date": "20180830",
      "report_date": "20180131",
      "code_info": "Lot numbers: 47883, 47910 & 47911"
    }
  ]
}