{
  "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": [
    {
      "country": "United States",
      "city": "Mounds View",
      "address_1": "8200 Coral Sea St Ne",
      "reason_for_recall": "Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's after a ride-through POR reset.",
      "address_2": "",
      "product_quantity": "21,685",
      "code_info": "Model Number: LNQ22",
      "center_classification_date": "20210714",
      "distribution_pattern": "Worldwide distribution - US Nationwide in the states of AK, AL, AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, PA, SC, SD, TN, TX,  UT, VA, VT, WA, WI, and WY. The countries of Australia, Austria, Canada, Denmark, Finland, Germany, Ireland, Italy, Netherlands, Netherlands Antilles, Sweden, Switzerland, and United Kingdom.",
      "state": "MN",
      "product_description": "Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only",
      "report_date": "20210721",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)",
      "recall_number": "Z-2076-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "88089",
      "more_code_info": "",
      "recall_initiation_date": "20210514",
      "postal_code": "55112-4391",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}