{
  "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": "Cartridges may contain individual discs which were not impregnated with antibiotic.",
      "address_2": "",
      "product_quantity": "9 packs",
      "code_info": "Lot 1275353, Exp. 31Dec2015",
      "center_classification_date": "20140121",
      "distribution_pattern": "Nationwide Distribution: US including Puerto Rico.",
      "state": "KS",
      "product_description": "Oxoid Antimicrobial Susceptibility Test Discs, Cefpodoxime 10 mcg., CT1612B, packaged in cartridges of 50 discs, 5 cartridges/pack. 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 to assist in the determination of a suitable antibiotic agent for treatment purposes",
      "report_date": "20140129",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Remel Inc",
      "recall_number": "Z-0792-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "65184",
      "termination_date": "20140121",
      "more_code_info": "",
      "recall_initiation_date": "20130409",
      "postal_code": "66215-3519",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}