{
  "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": "2026-04-01",
    "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": "84693",
      "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": "Telephone",
      "distribution_pattern": "US Distribution to IL.",
      "recall_number": "Z-0863-2020",
      "product_description": "Custom Healthcare Systems, Inc. Inpatient Dialysis Kit PAK-19244.  Single use.    Dialysis kit",
      "product_quantity": "240 kits",
      "reason_for_recall": "A component (1961 TELFA PAD 2 X 3) contains LATEX and was used in the Medical Convenience Kit(PAK-19244). Case label and device label for product did NOT show that the Medical Convenience Kit contained LATEX.",
      "recall_initiation_date": "20191220",
      "center_classification_date": "20200124",
      "termination_date": "20220801",
      "report_date": "20200205",
      "code_info": "LOT NUMBER: 20190614, expires February 1, 2020  UNIQUE DEVICE IDENTIFIER: (01)00811870033261(17)200201(10)20190614"
    }
  ]
}