{
  "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": "Terminated",
      "city": "Alameda",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84866",
      "recalling_firm": "Abbott Diabetes Care, Inc.",
      "address_1": "1360 S Loop Rd",
      "address_2": "N/A",
      "postal_code": "94502-7000",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: KY, NY, TN, MA, IL, SC, VT, FL, CA, NC, MS, NJ, TX, AL, GA, OK, CT, PA, NE, ND, MT, MO, DC, ME, LA, KS, ID, OH, MN, NM, VA, IN",
      "recall_number": "Z-1558-2020",
      "product_description": "FreeStyle Precision H Blood Glucose and Ketone Monitoring System, UDI: 00093815711810",
      "product_quantity": "N/A",
      "reason_for_recall": "Instructions sent in a letter or in instructions for use for disinfecting blood glucose and/or ketone meters were distributed but not cleared by the U.S. FDA, and devices were not cleared for multiple-patient use. Instructions could lead to inappropriate meter disinfection or improper handling of contaminated meters, which may cause infection or exacerbation of an existing infection.",
      "recall_initiation_date": "20191114",
      "center_classification_date": "20200323",
      "termination_date": "20210428",
      "report_date": "20200401",
      "code_info": "All lots.",
      "more_code_info": ""
    }
  ]
}