{
  "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": [
    {
      "status": "Terminated",
      "city": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76327",
      "recalling_firm": "Covidien LLC",
      "address_1": "60 Middletown Ave",
      "address_2": "N/A",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-1409-2017",
      "product_description": "Premier Guard Drape, Sterile.  For Use with Verisphere (01-0035) and ArQ.Sphere (01-0044)    Item Number: 01-0037  Used in conjunction RF Surgical Gauze detection systems to protect scanning device from contamination during various surgical procedures",
      "product_quantity": "42,750 units",
      "reason_for_recall": "Sterility compromised due to breach in sterile barrier",
      "recall_initiation_date": "20170123",
      "center_classification_date": "20170304",
      "termination_date": "20190807",
      "report_date": "20170315",
      "code_info": "Lot Numbers: 1410577-4 to 1605778"
    }
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}