{
  "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": [
    {
      "status": "Terminated",
      "city": "Durham",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70690",
      "recalling_firm": "TEM Systems Inc",
      "address_1": "4309 Emperor Blvd Ste 100",
      "address_2": "N/A",
      "postal_code": "27703-8069",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-1379-2015",
      "product_description": "ROTROL P Control for ROTEM delta Thromboelastometry System, Manufactured for: Tem Innovations GmbH.",
      "product_quantity": "Total 1574 x 5 vials per box",
      "reason_for_recall": "Some of vials were found to be partially filled.",
      "recall_initiation_date": "20141023",
      "center_classification_date": "20150403",
      "termination_date": "20150813",
      "report_date": "20150415",
      "code_info": "Article number 503-25 (US ROTROL P), Lot no. 41819801, exp date 2016-11 and Lot no. 41855701, exp date 2017-06."
    }
  ]
}