{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Edison",
      "address_1": "23 Nevsky St",
      "reason_for_recall": "Test results may be erroneously elevated or report an out-of-range high (OOR-H) error code in non heparinized blood samples.",
      "address_2": "",
      "product_quantity": "US- 315 cuvettes; OUS - 2835 cuvettes",
      "code_info": "Lot Number A4JCA001",
      "center_classification_date": "20140721",
      "distribution_pattern": "Worldwide Distribution - US including the states of Georgia, Virginia and New York., and the countries of Canada, France, Italy, Liechtenstein and Romania.",
      "state": "NJ",
      "product_description": "Hemochron Jr. Whole Blood Microcoagulation System APTT Cuvette. For in vitro diagnostic coagulation test.  Catalog number J103.",
      "report_date": "20140730",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ITC-Nexus Dx",
      "recall_number": "Z-2088-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68659",
      "termination_date": "20141211",
      "more_code_info": "",
      "recall_initiation_date": "20140620",
      "postal_code": "08820-2425",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}