{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Greenville",
      "address_1": "10 S Academy St",
      "reason_for_recall": "Software design error in IMPAX CV 7.8 SU3",
      "address_2": "",
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      "code_info": "Softwaer version: IMPAX CR 7.8 SU3 Optical Character Recognition (OCR) Service",
      "center_classification_date": "20130408",
      "distribution_pattern": "Distribute in the state of FL and  KY",
      "state": "SC",
      "product_description": "IMPAX CV 7.8 SU3 - OCR Service.    The IMPAX CV Reporting component facilitates the quick , effective creation of digital structured reports for adult catheterization and echocardiography, pediatric echocardiography, congenital heart disease, nuclear cardiology and non-invasive vascular disease management.",
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      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "AGFA Corp.",
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      "product_type": "Devices",
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      "termination_date": "20140401",
      "more_code_info": "",
      "recall_initiation_date": "20130315",
      "postal_code": "29601-2632",
      "voluntary_mandated": "Voluntary: Firm initiated",
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