{
  "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": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73494",
      "recalling_firm": "Medtronic Inc.",
      "address_1": "8200 Coral Sea St Ne",
      "address_2": "N/A",
      "postal_code": "55112-4391",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "Worldwide Distribution-US (nationwide) including DC and the countries of Andorra, Australia, Austria, Belgium, Botswana, Brunei Darussalam, Bulgaria, Canada, China, Colombia, Croatia, Czech Republic,  Denmark, Faroe Islands , Finland, France, Germany, Greece, Hong Kong,  Hungary, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Kazakhstan, Kenya,  Kuwait, Latvia, Lithuania, Luxembourg, Malaysia, Malta, Martinique, Namibia,  Netherlands, New Caledonia, New Zealand, Norway, Oman, Philippines,   Poland, Portugal, Qatar, Russian Federation, Saudi Arabia, Serbia, Singapore,  Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Tanzania,  Thailand, Turkey, United Arab Emirates and United Kingdom.",
      "recall_number": "Z-1249-2016",
      "product_description": "Reveal LINQ insertable Cardiac Monitor, Model LNQ11.  Monitors subcutaneous ECG continuously.",
      "product_quantity": "189,009",
      "reason_for_recall": "Medtronic has identified an issue with the sensitivity of an algorithm used in the Reveal LINQ ICM that may prematurely trigger the Recommended Replacement Time (RRT) alert in some devices. Battery capacity is not affected and the device will continue to support data collection and manual data transmissions. As part of the normal behavior of the device, 30 days after RRT status is reached, Reveal",
      "recall_initiation_date": "20160223",
      "center_classification_date": "20160325",
      "termination_date": "20170925",
      "report_date": "20160406",
      "code_info": "All Reveal LINQ ICM, Model LNQ11 serial numbers are impacted. Medtronic continues to manufacture and distribute Reveal Ll NQ devices."
    }
  ]
}