{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Greensboro",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77282",
      "recalling_firm": "ConvaTec, Inc",
      "address_1": "7900 Triad Center Dr Ste 400",
      "address_2": "N/A",
      "postal_code": "27409-9076",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA, CT, FL, GA, IL, MO, NJ, NY, NC, OH, PA, RI, VA , Puerto Rico, Australia, Belgium, Canada, Columbia, Czech, Denmark, Finland, France, Germany, Greece, Israel, Italy, Japan, Jordan, Malaysia, Malta, Netherlands, Norway, Rwanda, Saudi Arabia, Sweden, Switzerland, United Kingdom,  and Vietnam",
      "recall_number": "Z-2244-2017",
      "product_description": "Non-Rebreather Mask w 7\u0019 (2.1 m) \u001cNo-Crush\u001d Tubing, Adult, Product Code 9106-E, Product Code 9108-E, Product Code ZRNRMA",
      "product_quantity": "N/A",
      "reason_for_recall": "",
      "recall_initiation_date": "20170510",
      "center_classification_date": "20170602",
      "termination_date": "20210827",
      "report_date": "20170614",
      "code_info": "Lot Number (Product Code 9106-E) 100168, 101193, 101896; (Product Code 9108-E) 102143, 103119, 103378, 104273, 104839, 104879, 105224; (Product Code ZRNRMA) 101060, 103355, 104768, 105655"
    }
  ]
}