{
  "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": "The firm is recalling the product because the cartridges may contain discs that have an insufficient dose of antibiotic.",
      "address_2": "",
      "product_quantity": "23 units",
      "code_info": "Lot 1186069",
      "center_classification_date": "20130212",
      "distribution_pattern": "US Nationwide Distribution including the states of: CA, CT, GA, IA, KS, OK, RI, TX, WA, WI,",
      "state": "KS",
      "product_description": "Oxoid Antimicrobial Susceptibility Discs, Cefoxitin 30ug REF CT0119B, packaged with 50 discs per cartridge, 5 cartridges per box.  The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hants, UK.",
      "report_date": "20130220",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Remel Inc",
      "recall_number": "Z-0808-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63556",
      "termination_date": "20130604",
      "more_code_info": "",
      "recall_initiation_date": "20120821",
      "postal_code": "66215-3519",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}