{
  "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": [
    {
      "country": "United States",
      "city": "Abbott Park",
      "address_1": "100 Abbott Park Rd Bldg Ap8b",
      "reason_for_recall": "Devices were delivered without the required dry ice.",
      "address_2": "",
      "product_quantity": "1 unit",
      "code_info": "LN 4P72-01; Lot 902920500",
      "center_classification_date": "20190516",
      "distribution_pattern": "Distribution to Latvia.",
      "state": "IL",
      "product_description": "ARCHITECT HbA1C Calibrators - Product Usage: The ARCHITECT HbA1c Calibrators are for the calibration of the ARCHITECT i System when used for the quantitative determination of percent hemoglobin A1c (HbA1c) in human whole blood.",
      "report_date": "20190522",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Abbott Laboratories",
      "recall_number": "Z-1356-2019",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "82590",
      "termination_date": "20191220",
      "more_code_info": "",
      "recall_initiation_date": "20190409",
      "postal_code": "60064-3502",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}