{
  "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": "2026-04-22",
    "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": "70471",
      "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": "US Distribution to the states of :  MI, ND, SC, TN, and TX.",
      "recall_number": "Z-1232-2015",
      "product_description": "Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials.  The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England and Oxoid Ltd., Basingstoke, Hants, England.",
      "product_quantity": "24 packs (10 x 100 ml vials)",
      "reason_for_recall": "Use of the product may not provide adequate recovery and could result in false negative identification of Legionella pneumophila.",
      "recall_initiation_date": "20150205",
      "center_classification_date": "20150302",
      "termination_date": "20170213",
      "report_date": "20150311",
      "code_info": "Lot No. 1545171"
    }
  ]
}