{
  "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": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "10020 Pacific Mesa Blvd",
      "reason_for_recall": "CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP 9230, because they may have a defect in the trifurcated component that could result in a component leak.",
      "address_2": "",
      "product_quantity": "9,550 units",
      "code_info": "Trifurcated Extension Set, Model No. ME 1224,   Lot No.  11066540  11075718  11085047  11086237  11086676  11095178  11096312  11106045  11126756  12025801  12037064  12037127  12065225  12065586  12076327  12095460  13025322  13035514  13076233  13085002    Trifurcated Extension Set, Model No. MP 9230  Lot No. 13015666.",
      "center_classification_date": "20140204",
      "distribution_pattern": "Nationwide in US and Canada",
      "state": "CA",
      "product_description": "Trifurcated Extension Set, model no. ME 1224.  Trifurcated Extension Set, model no. MP 9230.",
      "report_date": "20140212",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CareFusion 303, Inc.",
      "recall_number": "Z-0931-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67326",
      "termination_date": "20140806",
      "more_code_info": "",
      "recall_initiation_date": "20140116",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}