{
  "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": "Bedford",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66894",
      "recalling_firm": "Instrumentation Laboratory Co.",
      "address_1": "180 Hartwell Road",
      "address_2": "N/A",
      "postal_code": "01730-2443",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-0514-2014",
      "product_description": "HemosIL Normal Control 1 UNASSAYED  Part Number: 0020003120",
      "product_quantity": "80319 Kits",
      "reason_for_recall": "HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks 510(k) approval",
      "recall_initiation_date": "20131115",
      "center_classification_date": "20131216",
      "termination_date": "20140325",
      "report_date": "20131225",
      "code_info": "All lots"
    }
  ]
}