{
  "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": "69771",
      "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 to FL",
      "recall_number": "Z-0578-2015",
      "product_description": "Oxoid Legionella BCYE Growth Supplement packaged in packs of 10-100ml vials.      A growth supplement for the isolation of Legionella.",
      "product_quantity": "1/10/100 ml/vials/packs",
      "reason_for_recall": "Use of the product could result in inadequate recovery of Legionella pneumophila which could result in false negative reporting.",
      "recall_initiation_date": "20141113",
      "center_classification_date": "20141210",
      "termination_date": "20150129",
      "report_date": "20141217",
      "code_info": "Lot number: 1374439, Exp: 31 Aug 2015"
    }
  ]
}