{
  "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": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64204",
      "recalling_firm": "Carefusion 303 Inc",
      "address_1": "3750 Torrey View Ct",
      "address_2": "N/A",
      "postal_code": "92130-2622",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including the states of  AK, CA, CO, IL, MO, NV, NY, TX and UT.",
      "recall_number": "Z-0832-2013",
      "product_description": "CareFusion SmartSite Gravity Blood Set Model 42082E.   Used to administer blood and blood products through a needle or catheter inserted into the patient's artery or vein.",
      "product_quantity": "5,050 units",
      "reason_for_recall": "CareFusion is recalling the SmartSite¿ Gravity Blood Set as a result of a potential for separation at the connection of the drip chamber and tubing . The separation may be observed at priming or observed during use. If a separation between the drip chamber and tubing occurs, this could cause a delay in treatment.",
      "recall_initiation_date": "20121220",
      "center_classification_date": "20130215",
      "termination_date": "20130725",
      "report_date": "20130227",
      "code_info": "Lot number 12055225"
    }
  ]
}