{
  "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": [
    {
      "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": "7200",
      "code_info": "GTIN Primary Package: 20884522033234  GTIN Secondary Package: 10884522033237    Lot Number: 20J0699FAX",
      "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": "Mechanical Filter with Connector Small, Tethered Cap, Item Code 351/5979 - 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-1867-2021",
      "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"
    }
  ]
}