{
  "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": [
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      "status": "Terminated",
      "city": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84991",
      "recalling_firm": "Covidien Llc",
      "address_1": "15 Hampshire St",
      "address_2": "N/A",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide domestic distribution. Foreign distribution to Australia, Canada, Austria  Belgium  Canary Islands  Czech Republic  Denmark  Finland  France  Germany  Greece  Hungary  Italy  Jordan  Kazakhstan  Kenya  Lithuania  Luxembourg  North Macedonia  Poland  Portugal  Reunion  Romania  Russian Federation  Serbia  Slovakia  Spain  Sweden  Switzerland  United Kingdom  No U.S. distribution of Kits. Foreign distribution in EMEA  only. (Europe, Middle East and Africa.)",
      "recall_number": "Z-1446-2020",
      "product_description": "Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084  20884524000081; 10884524001937  20884524001934",
      "product_quantity": "70361",
      "reason_for_recall": "Sterile packaging may potentially be compromised, and use of products may result in increased risk for infection.",
      "recall_initiation_date": "20200210",
      "center_classification_date": "20200305",
      "termination_date": "20240426",
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