{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Plymouth",
      "address_1": "5050 Nathan Ln N",
      "reason_for_recall": "High rate of reported complaints for the loss of contact force information while using the TactiCath Quartz Contact Force Ablation Catheter",
      "address_2": "",
      "product_quantity": "84104 devices",
      "code_info": "All batch numbers with an expiration date of April 25, 2020",
      "center_classification_date": "20200709",
      "distribution_pattern": "Worldwide distribution.",
      "state": "MN",
      "product_description": "TactiCath Quartz Contact Force Ablation Catheter, Model Numbers:  PN-004 065 (GTIN 07640157990033) and PN-004 075 (GTIN 07640157990040) - Product Usage: is a multi-electrode irrigated catheter with a deflectable tip designed to allow electrophysiological mapping of the heart and, when connected to an RF generator, to deliver radiofrequency current to the catheter tip electrode for the purpose of ablation.",
      "report_date": "20200715",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Abbott",
      "recall_number": "Z-2541-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "85775",
      "termination_date": "20210211",
      "more_code_info": "",
      "recall_initiation_date": "20200522",
      "postal_code": "55442-3209",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}