{
  "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": "Lenexa",
      "state": "KS",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71614",
      "recalling_firm": "Remel Inc",
      "address_1": "12076 Santa Fe Trail Dr",
      "address_2": "N/A",
      "postal_code": "66215-3519",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution, including Puerto Rico and the country of Canada.",
      "recall_number": "Z-2350-2015",
      "product_description": "PathoDx Strep Grouping Kit, REF 62025, packaged 60 tests per kit.      Latex agglutination test for identification of beta-hemolytic streptococci of Lancefield Groups A, B, C, F or G from primary culture plates.",
      "product_quantity": "1859 kits",
      "reason_for_recall": "A reagent present may produce weak or slow reactions; continued use may result in a failure to identify target species.",
      "recall_initiation_date": "20150630",
      "center_classification_date": "20150807",
      "termination_date": "20170213",
      "report_date": "20150819",
      "code_info": "lot 1470133, exp. date 31 Mar 2016"
    }
  ]
}