{
  "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": [
    {
      "country": "United States",
      "city": "Lenexa",
      "address_1": "12076 Santa Fe Trail Dr",
      "reason_for_recall": "Use of affected lots may give false indication of susceptibility to Nitrofurantoin.",
      "address_2": "",
      "product_quantity": "60 packs",
      "code_info": "Lots 1194944 and 1198342",
      "center_classification_date": "20130826",
      "distribution_pattern": "US Distribution including the states of  AL, AR, CA, FL, GA, IL, KS, LA, MA, MD, NY, OK, PA, RI, TX, VA, and WA.",
      "state": "KS",
      "product_description": "Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin), Cat. #CT0036B, packaged in cartridges of 50 discs, 5 cartridges/pack.  The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England    Product is used in the semi-quantitative agar diffusion test method for in-vitro susceptibility testing.",
      "report_date": "20130904",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Remel Inc",
      "recall_number": "Z-2081-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64852",
      "termination_date": "20140603",
      "more_code_info": "",
      "recall_initiation_date": "20130325",
      "postal_code": "66215-3519",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}