{
  "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": {
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    {
      "status": "Terminated",
      "city": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
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      "address_1": "3545 SW 47th Ave",
      "address_2": "N/A",
      "postal_code": "32608-7691",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S Distribution: AK, AL, CA, CO, FL, IL, IN, KY, MA, MI, NY, OH, OR, PA, TN, TX and WV. *** Foreign: Australia, Canada, France, United Kingdom, Italy, Japan, Netherlands, Saudi Arabia, India and Thailand.",
      "recall_number": "Z-1440-2020",
      "product_description": "Monitor for the Functional Imaging System for Magnetic Resonance Imaging System",
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      "reason_for_recall": "Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.",
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      "report_date": "20200311",
      "code_info": "9896-032-0815 SensaVue HD and 9896-032-0872x SensaVue fMRI"
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}