{
  "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": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89677",
      "recalling_firm": "Volcano Corp",
      "address_1": "3721 Valley Centre Dr Ste 500",
      "address_2": "N/A",
      "postal_code": "92130-3328",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: CO, GA, MA, TX, AZ, NY, PA, CA, FL, MO, OR, MD, NC, TN    OUS: JP, DE, GB, NL, IT",
      "recall_number": "Z-0901-2022",
      "product_description": "IntraSight Mobile IVUS Systems, Model: 797415, Part numbers: 300002018101, 300002018102",
      "product_quantity": "47",
      "reason_for_recall": "Multi-Modality Touch Screen Modules (MM-TSM), which are bedside/secondary control units, used as part of Mobile IVUS systems, are missing the following labeling information: Unique Device Identifier, Legal Manufacturer Information, Part Number, Rx Symbol, and Model Reference Information.",
      "recall_initiation_date": "20220124",
      "center_classification_date": "20220408",
      "report_date": "20220420",
      "code_info": "All MM-TSM units, Device Identifier (DI): 00845225012915"
    }
  ]
}