{
  "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": "76840",
      "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": "Letter",
      "distribution_pattern": "AL, CA, DC, FL, GA, HI, IL, IN, KS, LA, MA, MN, MO, NV, NJ, NM, NY, OH, OK, OR, SC, TN, TX, VA, and Canada",
      "recall_number": "Z-1738-2017",
      "product_description": "DX-D600 - DXD Imaging Package",
      "product_quantity": "81 units",
      "reason_for_recall": "One of the dent markers from the DX-D600 dropped down from the overhead rail.",
      "recall_initiation_date": "20160502",
      "center_classification_date": "20170405",
      "termination_date": "20170410",
      "report_date": "20170412",
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