{
  "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": "Lake Forest",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73461",
      "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": "US Distribution in the state of CA.",
      "recall_number": "Z-1908-2016",
      "product_description": "ABG-HM-1 Hummi Micro Draw Blood Transfer Device; Used for blood transfer and collection from peripheral arterial line catheters.",
      "product_quantity": "62,400",
      "reason_for_recall": "Hummingbird Med Devices, Inc. is recalling the Hummi Micro Draw because of insertion difficulties.",
      "recall_initiation_date": "20150311",
      "center_classification_date": "20160705",
      "termination_date": "20170207",
      "report_date": "20160713",
      "code_info": "Lot Numbers:  20140510  20140513  20140516  20140519  20140603  20140606  20140609  20140612  14299"
    }
  ]
}