{
  "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": [
    {
      "country": "United States",
      "city": "Andover",
      "address_1": "6 Tech Dr",
      "reason_for_recall": "Dual Hemo MCable Pods with Revision  Index (RI) 15 and 16, which are used with the Dr¿ger Infinity Acute Care System, may  permit liquid ingress inconsistent with their IPX4 rating, which could potentially result in an  incorrect measured value of invasive blood pressure.",
      "address_2": "",
      "product_quantity": "2,760",
      "code_info": "Have the affected revision indexes: 15 or 16 (found on the product label)",
      "center_classification_date": "20180309",
      "distribution_pattern": "Nationally",
      "state": "MA",
      "product_description": "INFINITY DUAL HEMO MCable Pod",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Draegar Medical Systems, Inc.",
      "recall_number": "Z-0942-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79209",
      "termination_date": "20180615",
      "more_code_info": "",
      "recall_initiation_date": "20171004",
      "postal_code": "01810-2434",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}