{
  "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": "Waukesha",
      "address_1": "3000 N Grandview Blvd",
      "reason_for_recall": "GE Healthcare has become aware through complaints of a potential safety issue with its Invasive Blood Pressure Cable made for use with a Spectramed / BD invasive blood pressure transducer. Due to use of an incorrect O-ring, the mating of the cable with the transducer is faulty. This situation inhibits blood pressure measurement from being monitored correctly.",
      "address_2": "",
      "product_quantity": "279",
      "code_info": "Product ID Number       Lot Code    2016995-001                   xxxx2010E  2016995-002 xxxx2010D  2016995-003 xxxx2010C  2016995-004                  xxxx2010C",
      "center_classification_date": "20120716",
      "distribution_pattern": "Worldwide Distribution -- USA (nationwide)  including the states  of AK, CA, IL, MS, NJ, PR, SD, TN, TX, and  VA. and the countries of  ARGENTIAN, AUSTRALIA, BELGIUM, CHINA, GERMANY, ALGERIA, ECUADOR, EGYPT, FINLAND, UNITED KINGDOM, JORDAN, JAPAN, MOROCCO, MAURITUS, NETHERLANDS, OMAN, PERU, SEBIA, SUDI ARABIA, SINGAPORE, EL SALVADOR, TURKEY, URUGUAY and  SOUTH AFRICA.",
      "state": "WI",
      "product_description": "GE Healthcare, Invasive Blood Pressure Care Cables.    Product ID Number: 2016995-001, 2016995-002, 2016995-003, 2016995-004.",
      "report_date": "20120725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Healthcare, LLC",
      "recall_number": "Z-2015-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62123",
      "termination_date": "20131205",
      "more_code_info": "",
      "recall_initiation_date": "20120612",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}