{
  "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": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73315",
      "recalling_firm": "CareFusion 303, Inc.",
      "address_1": "10020 Pacific Mesa Blvd",
      "address_2": "N/A",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in US: AR, AZ, CA, FL, GA, IN, KY, MD, MI, MN, MO, NJ, NM, NY, OH, OR, PA, SC, TN, TX, VA, WI.",
      "recall_number": "Z-1239-2016",
      "product_description": "Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092",
      "product_quantity": "170 units",
      "reason_for_recall": "CareFusion is recalling the Alaris PC unit because a component on the PC unit power supply may cause a \"System Error\" or \"Missing Battery\" error code (120.4630).",
      "recall_initiation_date": "20160212",
      "center_classification_date": "20160324",
      "termination_date": "20170623",
      "report_date": "20160330",
      "code_info": "Serial No.  4044845  9950535  4064411  12475162  4045659  9899143  3606478  4021398  4093501  4043745  4063430  4094994  9907675  9945292  9922622  4043375  12409069  4020663  12498854  4044531  4058193  12351849  4064030  9925068  12426138  4063830  4063911  9945269"
    }
  ]
}