{
  "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": [
    {
      "country": "United States",
      "city": "Indianola",
      "address_1": "1 Bayer Dr",
      "reason_for_recall": "Software Version SW 005.006_SH,  resulted in the removal of purge enforcement from traditional New-Case, Power Up and Syringe Change use cases while the injector head is in the upright position.",
      "address_2": "",
      "product_quantity": "71",
      "code_info": "Catalog numbers: ART 700 PEDL, ART 700 TABL, ART 700 OCS, which utilize Software Version SW 005.006_SH.    Affected serial numbers: 20329, 20570, 101148, 20392, 20425,  20427, 30046, 100945, 100186, 21255, 30086, 20025, 101153,  101159, 20714, 100873, 20437, 100033, 100249, 20333, 100511,  101206, 100002, 100890, 101208, 20323, 20914, 20342, 10172,  10074, 20195, 20196, 20850, 20929, 101106, 30020, 30024, 30033,  20252, 10087, 20851, 100009, 100864, 100335, 10095, 20302, 20306,  100013, 20918, 100141, 20158, 100784, 20735, 20422, 101149,  20842, 20018, 101114, 100056, 100075, 20434, 21024, 20311, 20763,  10055, 20786, 20701, 20729, 20040, 100092, 20501",
      "center_classification_date": "20150916",
      "distribution_pattern": "Worldwide Distribution. US Nationwide, Germany, France, UK, Netherlands, Sweden, and Canada.",
      "state": "PA",
      "product_description": "Angiographic Injector. Medrad Mark 7 Arterion Injection System, which utilizes Software Version SW 005.006_SH; to be used specifically for the purposes of injecting contrast medium and common flushing solutions into humans for angiographic studies.",
      "report_date": "20150923",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Bayer Healthcare",
      "recall_number": "Z-2775-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71994",
      "termination_date": "20160817",
      "more_code_info": "",
      "recall_initiation_date": "20150804",
      "postal_code": "15051-9702",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}