{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Richmond",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81179",
      "recalling_firm": "Custom Healthcare Systems, Inc.",
      "address_1": "4205 Eubank Rd",
      "address_2": "N/A",
      "postal_code": "23231-4328",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Connecticut, Georgia, Kentucky, North Carolina, Virginia, Maryland, Oklahoma, Illinois, South Carolina,",
      "recall_number": "Z-0242-2019",
      "product_description": "CHS Custom Convenience Kit-  (1) DT\tSCATPAD, DBL. TAPE, 12.5  X 16.5 \t  Product Number: SEPA 402  (2) SCATPAD, 11  X 34 \t  Product Number: SPA502",
      "product_quantity": "(1) 750 units (2) 200 units",
      "reason_for_recall": "Convenience kits were sealed in immediate Tyvek pouches using incorrect specifications compromising product sterility",
      "recall_initiation_date": "20180813",
      "center_classification_date": "20181025",
      "termination_date": "20220801",
      "report_date": "20181031",
      "code_info": "(1)Lot Number:72018   Exp. Date: 7/1/2021  (2) Lot number: 71118  Exp. Date: 7/1/2021"
    }
  ]
}