{
  "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": [
    {
      "country": "United States",
      "city": "North Haven",
      "address_1": "60 Middletown Ave",
      "reason_for_recall": "The company was notified by their supplier of sterilization services for airway products in Italy of potential deviations from validated parameters for ethylene oxide sterilization.",
      "address_2": "",
      "product_quantity": "10890",
      "code_info": "GTIN Primary Package: 10884521779372  GTIN Secondary Package: 20884521779379    Lot Numbers: 19F0869FAX  19F0870FAX  20G1669FAX  20G1670FAX  20H0377FAX",
      "center_classification_date": "20210616",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of DE, KY, NY, TX, VA, VT, and WA.  Global Distribution.",
      "state": "CT",
      "product_description": "HME for Tracheostomized Patients, Item Code 353S13046 - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors.",
      "report_date": "20210623",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Covidien, LP",
      "recall_number": "Z-1869-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "87925",
      "more_code_info": "",
      "recall_initiation_date": "20210429",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}