{
  "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": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72406",
      "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": "Distributed in PR and the states of MO, NC, GA, MS, LA, and KY.",
      "recall_number": "Z-0265-2016",
      "product_description": "MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.",
      "product_quantity": "15",
      "reason_for_recall": "Display freeze of MODULARIS hand control results in information not being updated on the display. Current treatment data is not shown to the user.",
      "recall_initiation_date": "20150924",
      "center_classification_date": "20151112",
      "termination_date": "20161205",
      "report_date": "20151118",
      "code_info": "model# 1157200"
    }
  ]
}