{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87904",
      "recalling_firm": "Abbott Laboratories Inc. (St Jude Medical)",
      "address_1": "1 Saint Jude Medical Dr",
      "address_2": "",
      "postal_code": "55117-1789",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "US Nationwide distribution in the states of MI, KS, MO, TX.",
      "recall_number": "Z-1854-2021",
      "product_description": "v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris\" System Display,    Model H700124, The WorkMate Claris\" System is a computer-based electrocardiographic recording and monitoring system designed for efficient capture, display, and retrieval of surface and intracardiac signals during cardiac EP studies.",
      "product_quantity": "9 units",
      "reason_for_recall": "Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.",
      "recall_initiation_date": "20210505",
      "center_classification_date": "20210614",
      "termination_date": "20240618",
      "report_date": "20210623",
      "code_info": "Serial Numbers:  14774202, 14779111, 15812169, 15812170, 18243196, 18243205, 18643643, 18782716, 18917926",
      "more_code_info": ""
    }
  ]
}