{
  "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": "67777",
      "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": "Distribution was made to CA, FL, IL, MA, ME, NJ, PA, TN, TX, VA, and VT.  There was no foreign/military/government distribution.",
      "recall_number": "Z-1473-2014",
      "product_description": "Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box.  The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, DR0802.  The responsible firm on the label is Oxoid Ltd., Basingstoke, Hants, England.",
      "product_quantity": "72/50-test boxes",
      "reason_for_recall": "A reagent contained within the product may return false negative results.",
      "recall_initiation_date": "20140317",
      "center_classification_date": "20140418",
      "termination_date": "20141211",
      "report_date": "20140430",
      "code_info": "DR0800M box lot numbers 1314413, Exp. 30Jun2014, and 1301907, Exp. 31May2014; DR0802 reagent bottle lot number 1265366, exp. June 2014",
      "more_code_info": ""
    }
  ]
}