{
  "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": "Greenville",
      "state": "SC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77629",
      "recalling_firm": "AGFA Healthcare Corp.",
      "address_1": "10 S Academy St",
      "address_2": "N/A",
      "postal_code": "29601-2632",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide Distribution to NJ, NC, OH, PA, SC, TN, TX, and WI",
      "recall_number": "Z-2652-2017",
      "product_description": "IMPAX Cardiovascular  The IMPAX CV Reporting module consists of a database and graphical user interface (GUI) that allows users to document procedure and clinical findings as structured data, with representation in printed or electronic formats",
      "product_quantity": "10",
      "reason_for_recall": "A customer experienced when using IMPAX CV Reporting software, specifically, when building a NIV report, the NIV Cardio report was showing incorrect findings for Aneurysm.",
      "recall_initiation_date": "20161222",
      "center_classification_date": "20170629",
      "termination_date": "20210827",
      "report_date": "20170705",
      "code_info": "Versions CV 12.2 SU3, CV 12.2 SU4, CV 12.2 SU5 and CV 12.2 SU6"
    }
  ]
}