{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lenexa",
      "state": "KS",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98403",
      "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": "US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.",
      "recall_number": "Z-1474-2026",
      "product_description": "Campy CVA Medium 100/PK, R01272",
      "product_quantity": "97",
      "reason_for_recall": "Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.",
      "recall_initiation_date": "20260205",
      "center_classification_date": "20260226",
      "report_date": "20260304",
      "code_info": "UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026"
    }
  ]
}