{
  "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": "2026-03-18",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Greensboro",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90856",
      "recalling_firm": "ConvaTec, Inc",
      "address_1": "7815 National Service Rd Ste 600",
      "address_2": "N/A",
      "postal_code": "27409-9403",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0130-2023",
      "product_description": "ConvaTec Active Life, One-Piece Drainable Pouch, 3/4-2 1/2 in., 19-64mm, REF 400599. For the management of stoma output following a colostomy or ileostomy procedure.",
      "product_quantity": "2611 units",
      "reason_for_recall": "impaired functionality of the release liner",
      "recall_initiation_date": "20220816",
      "center_classification_date": "20221024",
      "report_date": "20221102",
      "code_info": "UDI/DI:  768455102907, Batch numbers:  2A03486, 2B00301",
      "more_code_info": ""
    }
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}