{
  "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": "Ottawa",
      "state": "Ontario",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "61147",
      "recalling_firm": "Epocal Inc",
      "address_1": "2060 Walkley Rd",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide Distribution in the state of CA.",
      "recall_number": "Z-2034-2012",
      "product_description": "epoc Blood Analysis BGEM Test Cards for use with the epoc(R) Blood Analysis System      Product Usage:  Usage:  epoc Blood Analysis BGEM Test Cards are used with the epoc(R) Blood Analysis System which is a POC testing system",
      "product_quantity": "8,650",
      "reason_for_recall": "Customer reported problem while performing incoming QC of newly received lot of test cards.  Liquid quality control results were found to be out of range.  Further investigation by Epocal determined that a portion of the test card lot (approximately 3000 cards) could potentially report low glucose results.",
      "recall_initiation_date": "20110628",
      "center_classification_date": "20120719",
      "termination_date": "20131218",
      "report_date": "20120725",
      "code_info": "Catalog #CT-1004-00-00, lot number 07-11087-00",
      "more_code_info": ""
    }
  ]
}