{
  "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": "Some of the discs may not be impregnated with the antibiotic.",
      "address_2": "",
      "product_quantity": "40/5/50-disc cartridge packages",
      "code_info": "Lot 1174497, exp. 2015/04",
      "center_classification_date": "20140320",
      "distribution_pattern": "Nationwide Distribution",
      "state": "KS",
      "product_description": "Oxoid Vancomycin 30 mcg, each cartridge contains 50 susceptibility discs, CT0058B.  The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England.    Used in the semi-quantitative agar diffusion test method for in-vitro susceptibility testing.",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Remel Inc",
      "recall_number": "Z-1246-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67590",
      "termination_date": "20140625",
      "more_code_info": "",
      "recall_initiation_date": "20140218",
      "postal_code": "66215-3519",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}