{
  "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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      "city": "Greenville",
      "state": "SC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68211",
      "recalling_firm": "AGFA Corp.",
      "address_1": "10 S Academy St",
      "address_2": "",
      "postal_code": "29601-2632",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-1662-2014",
      "product_description": "IMPAX CV Pediatric Echo Reporting, IMPAX CV Echo Measurement Import via Optical Character Recognition (OCR) Service IMPAX. For the  creation of digital structured reports for cardiovascular diagnostic studies such as echocardiography.",
      "product_quantity": "One",
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      "recall_initiation_date": "20140430",
      "center_classification_date": "20140527",
      "termination_date": "20140918",
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}