{
  "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": "69629",
      "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": "Worldwide Distribution to USA including AL, CA, CO, IA, MO, NC, NY, NV, OH, PA, SC, SD, TN, TX, VA, WI and Internationally to Canada.",
      "recall_number": "Z-0449-2015",
      "product_description": "Remel TB Potassium Permanganate (.5% Aqueous) 40192, packaged in 250 ml bottles, 5/pkg.    A stain for use in qualitative procedures as a counterstain in the fluorescent microscopic detection of mycobacteria.",
      "product_quantity": "79/5/250- packages/bottles/ml",
      "reason_for_recall": "The product may appear cloudy or discolored and may not perform correctly in presumptive diagnosis of mycobacterial disease.",
      "recall_initiation_date": "20141029",
      "center_classification_date": "20141124",
      "termination_date": "20150601",
      "report_date": "20141203",
      "code_info": "Lot: 293086  Expiration 01Apr2015",
      "more_code_info": ""
    }
  ]
}