{
  "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": "Greenville",
      "address_1": "10 S Academy St",
      "reason_for_recall": "Baseline pulmonary capillary wedge (PCW) pressure values from IMPAX CV Reporting Cardiac Catheterization module were not correctly transferring into the hospital's electronic health record (EHR) system.",
      "address_2": "",
      "product_quantity": "26",
      "code_info": "Model # L9M21000.  Software versions: IMPAX CV 7.8, 7.8 SU1, 7.8 SU2 and 7.8 SU3, IMPAX CV 7.8 SU2.5 with IMPAX  CV Outbound Report Stylesheet 7.8_HL",
      "center_classification_date": "20130408",
      "distribution_pattern": "Nationwide Distribution including the states of AK, GA, IL, KY, MA, NY, NC, RI, SC, TX, and VA.",
      "state": "SC",
      "product_description": "IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound Reporting.    Facilitates digital reports for catheterization, echocardiography,  and congenital heart disease.",
      "report_date": "20130417",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "AGFA Corp.",
      "recall_number": "Z-1070-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64656",
      "termination_date": "20140109",
      "more_code_info": "",
      "recall_initiation_date": "20130315",
      "postal_code": "29601-2632",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}