{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "10020 Pacific Mesa Blvd",
      "reason_for_recall": "CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set.",
      "address_2": "",
      "product_quantity": "5,760 units",
      "code_info": "Lot No. 13085603",
      "center_classification_date": "20160317",
      "distribution_pattern": "Michigan",
      "state": "CA",
      "product_description": "Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CareFusion 303, Inc.",
      "recall_number": "Z-1179-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73238",
      "termination_date": "20161024",
      "more_code_info": "",
      "recall_initiation_date": "20160215",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}