{
  "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": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73949",
      "recalling_firm": "Accriva Diagnostics Inc., dba ITC, dba Accumetrics",
      "address_1": "6260 Sequence Dr",
      "address_2": "N/A",
      "postal_code": "92121-4358",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. distribution to the following; state:  VA.   Foreign distribution to the following; China, Italy, Germany.",
      "recall_number": "Z-1720-2016",
      "product_description": "Accriva- APTT Cuvette for use on the Hemochron Jr. test system, catalog #J103, lot B6JCA012.",
      "product_quantity": "135 boxes",
      "reason_for_recall": "Clot activating reagent mis-positioned or visibly absent in the cuvette's test channel causing APTT test to either have an error code or an erroneously high result.",
      "recall_initiation_date": "20160422",
      "center_classification_date": "20160525",
      "termination_date": "20161214",
      "report_date": "20160601",
      "code_info": "Lot #B6JCA012"
    }
  ]
}