{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Bedford",
      "address_1": "180 Hartwell Rd",
      "reason_for_recall": "Prolonged clotting times",
      "address_2": "",
      "product_quantity": "722 kits",
      "code_info": "Lot # : 42255701",
      "center_classification_date": "20190906",
      "distribution_pattern": "States:  IL  WI  MI    Canada, Spain, Portugal, Poland, Italy, Israel, Switzerland, Denmark, Kazakhstan, United Kingdom, Germany, Netherlands, Belgium, France, Jordan, India, Hong Kong, Austria, Czechia, Australia, Sri Lanka, Argentina, Vietnam, Singapore, Japan, South Korea, Cyprus, Ireland, Hungary, Sweden, Serbia.",
      "state": "MA",
      "product_description": "ROTEM ex-tem  Rest of the world part No: 503-05 (ROW)",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Instrumentation Laboratory Co.",
      "recall_number": "Z-2487-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83523",
      "termination_date": "20200427",
      "more_code_info": "",
      "recall_initiation_date": "20190723",
      "postal_code": "01730-2443",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}