{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "A software error may result in a system crash.  The system must be restarted before the clinical procedure can be continued.  The ablation treatment must be performed with a different system or without the use of the interface.",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "Serial Number 120019",
      "center_classification_date": "20190223",
      "distribution_pattern": "The products were distributed to the following US states:  NJ.",
      "state": "PA",
      "product_description": "Sensis Vibe System, Model Number 11007642, with software version VD10B.",
      "report_date": "20190306",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-0936-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81959",
      "termination_date": "20200507",
      "more_code_info": "",
      "recall_initiation_date": "20181129",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}