{
  "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": "Augusta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74140",
      "recalling_firm": "Integrated Science Systems Inc",
      "address_1": "1215 George C Wilson Dr Unit A4",
      "address_2": "N/A",
      "postal_code": "30909-5700",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide distribution to CA only.",
      "recall_number": "Z-1911-2016",
      "product_description": "Sure Vue Color Staph 150T, Sure Vue Color Staph 300T, Sure Vue SELECT Staph, biokit SELECT Staph 75T   The product is used as an aid in the identification of Staphylococcus aureus from Culture",
      "product_quantity": "2625 kits",
      "reason_for_recall": "Customer complaints of very weak reactions with the kit, or false negative results with different Staph aureus cultures.",
      "recall_initiation_date": "20160219",
      "center_classification_date": "20160603",
      "termination_date": "20170228",
      "report_date": "20160615",
      "code_info": "Lot Numbers - KJ05016, KJ05017, KJ05018, KJ06019, KJ06020, KJ06021, KJ07023, KJ10028, J06022, KJ07024, KJ07025, KJ09026, KJ09027, KJ10029, KJ10030, KJ11034, KJ11035, KJ12040, KJ12041, KJ12042, KJ12043"
    }
  ]
}