{
  "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": "Edgewood",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72197",
      "recalling_firm": "Biochemical Diagnostics Inc",
      "address_1": "180 Heartland Blvd",
      "address_2": "N/A",
      "postal_code": "11717-8314",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0328-2016",
      "product_description": "CONSULT(TM) diagnostics hCG CONTROLS Kit, Part/Reorder Number 5011, IVD    Product Usage - CONSULT Diagnostics hCG Controls are intended to validate the performance of qualitative hCG urine procedures and immunochromatographic devices.",
      "product_quantity": "Domestic: 4,473 kits",
      "reason_for_recall": "CONSULT diagnostics hCG Controls have discrepant storage temperatures listed on the kit labels when compared with the individual vial labels and the package insert.",
      "recall_initiation_date": "20150914",
      "center_classification_date": "20151123",
      "termination_date": "20160126",
      "report_date": "20151202",
      "code_info": "Lot/Codes: KN165 (exp. 2017-09), KN169 (exp. 2017-10), KN171 (exp. 2017-11) and KN177 (exp. 2018-02)"
    }
  ]
}