{
  "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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  "results": [
    {
      "status": "Completed",
      "city": "Des Plaines",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90651",
      "recalling_firm": "Abbott Molecular, Inc.",
      "address_1": "1300 E Touhy Ave",
      "address_2": "",
      "postal_code": "60018-3315",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "There was only foreign distribution to Italy.",
      "recall_number": "Z-1518-2022",
      "product_description": "The Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use.",
      "product_quantity": "1",
      "reason_for_recall": "Incorrect optical calibration",
      "recall_initiation_date": "20220719",
      "center_classification_date": "20220812",
      "report_date": "20220824",
      "code_info": "Serial Number 00654",
      "more_code_info": ""
    }
  ]
}