{
  "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-1408-2017",
      "product_description": "Premier Guard Sterile Drape For Use with Blair-Port Wand (02-0029) and Blair-Port Wand X (01-0046)  Item Number: 01-0020    Used in conjunction RF Surgical Gauze detection systems to protect scanning device from contamination during various surgical procedures",
      "product_quantity": "1,111,600 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: 1112351 to 1609891"
    }
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}