{
  "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": "Lake Forest",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72350",
      "recalling_firm": "Hummingbird Med",
      "address_1": "20371 Lake Forest Dr Ste A6",
      "address_2": "N/A",
      "postal_code": "92630-8106",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of CA, KY, MD, GA, and  IL.",
      "recall_number": "Z-1636-2016",
      "product_description": "ABG-HM-1 Hummi Micro Draw Blood Transfer Device    Product Usage:  It is used for blood transfer and collection from Peripheral Arterial Line Catheters.",
      "product_quantity": "11500 units",
      "reason_for_recall": "Hummingbird Med Devices, Inc. is recalling ABG-HM-1 Hummi Micro Draw Blood Transfer because the connection between the \"Hummi\" Y connector and the yellow cannula hub may not be sufficiently secure enough and could separate while in use.",
      "recall_initiation_date": "20151001",
      "center_classification_date": "20160520",
      "termination_date": "20170126",
      "report_date": "20160601",
      "code_info": "Lot 15180, 15286, 15287, 15300, 15305"
    }
  ]
}