{
  "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": "Marburg",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83177",
      "recalling_firm": "DRG Instruments GmbH",
      "address_1": "Frauenbergstr. 18",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distribution to Canada",
      "recall_number": "Z-2410-2019",
      "product_description": "DRG Salivary Progesterone HS ELISA- IVD for the determination of progesterone in human saliva  REF: SLV-5911     in vitro diagnostic",
      "product_quantity": "8 Kits",
      "reason_for_recall": "Salivary Progesterone assay may observe a higher percentage of samples with low results. Saliva samples in the low measuring range of the kit {< 20 pg/ml) were assayed and producing a significantly lower result.",
      "recall_initiation_date": "20190606",
      "center_classification_date": "20190827",
      "termination_date": "20200511",
      "report_date": "20190904",
      "code_info": "Lot Number:315K029"
    }
  ]
}