{
  "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": "San Clemente",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77560",
      "recalling_firm": "ICU Medical, Inc.",
      "address_1": "951 Calle Amanecer",
      "address_2": "",
      "postal_code": "92673-6212",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution to Italy and France, and  the following states in the US: AZ, OH, TX, WA.",
      "recall_number": "Z-2719-2017",
      "product_description": "28 cm (11\") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, NanoClave¿, Rotating Luer.    Product Usage:  The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patient\u0019s vascular system through the administration set\u0019s needle or catheter (which is inserted into a vein).",
      "product_quantity": "6 units",
      "reason_for_recall": "The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.",
      "recall_initiation_date": "20170530",
      "center_classification_date": "20170711",
      "termination_date": "20240920",
      "report_date": "20170719",
      "code_info": "Lot No. 3296247.  Item No. 011-AM6117",
      "more_code_info": ""
    }
  ]
}