{
  "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": [
    {
      "status": "Terminated",
      "city": "McHenry",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84368",
      "recalling_firm": "Medela Inc",
      "address_1": "1101 Corporate Dr",
      "address_2": "N/A",
      "postal_code": "60050-7006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AL, AZ, CA, CO, FL, GA, IL, MN, MO, NC, NY, PA, SC, TN, TX, WA",
      "recall_number": "Z-0773-2020",
      "product_description": "Invia Foam Dressing Kit with FitPad - X-Large (3 pcs) SKU # 0876224.    The Invia Foam Dressing Kit with FitPad consists of a foam pad, a section interface (Invia FitPad) and Transparent Film (one or more pieces depending on the kit size).",
      "product_quantity": "331",
      "reason_for_recall": "Invia Foam Dressing Kit with FitPad could have holes in the sterile packaging.",
      "recall_initiation_date": "20191202",
      "center_classification_date": "20200102",
      "termination_date": "20201102",
      "report_date": "20200108",
      "code_info": "Lots:  17110012731 / Exp 17-Nov-19, 17110022736 / Exp 22-Nov-19, 17120012746 / Exp 8-Dec-19, 18010012767 / 4-Jan-20, 18070012913 / 31-Jul-20, 18090012960 / Exp 28-Sep-20, 18110013046 / 5-Nov-20."
    }
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}