{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mortsel",
      "state": "",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85028",
      "recalling_firm": "Agfa N.V.",
      "address_1": "Septestraat 27",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of FL, VA.",
      "recall_number": "Z-1502-2020",
      "product_description": "AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- a Tomographic X-ray system - Product Usage: TomoSynthesis is used to synthesize tomographic slices from a single tomographic sweep. The DR 800 is not intended for mammography applications",
      "product_quantity": "2 units",
      "reason_for_recall": "Tomosynthesis image acquisition sequence did not stop automatically after expected number of exposures.",
      "recall_initiation_date": "20200210",
      "center_classification_date": "20200318",
      "termination_date": "20230330",
      "report_date": "20200325",
      "code_info": "Serial Numbers:  00949, 1161",
      "more_code_info": ""
    }
  ]
}