{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83082",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "N/A",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-1897-2019",
      "product_description": "Siemens Artis zeego--Interventional Fluoroscopic X-Ray System  Model Number: 10280959",
      "product_quantity": "29",
      "reason_for_recall": "Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off,  can result in severe injuries to patients and operating personnel",
      "recall_initiation_date": "20190606",
      "center_classification_date": "20190628",
      "termination_date": "20210209",
      "report_date": "20190710",
      "code_info": "Serial Numbers:  160335  160430  160368  160469  160357  160370  160369  160509  160427  160433  160443  160428  160429  160463  160001  160461  160486  160800  160487  160488  160507  160840  160862  160856  160823  160914  160930  161235  160401"
    }
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}