{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Neenah",
      "address_1": "2100 Winchester Rd",
      "reason_for_recall": "Potential for tampon to come apart upon removal.",
      "address_2": "Po Box 349",
      "product_quantity": "68,852,076 units total",
      "code_info": "Package UPC: 36000426663;  Case UPC: 10036000426660;      Lot Numbers: NN629401B, NN629501A, NN631301B, NN631401A, NN631401B, NN632213A, NN632213B, NN703113B, NN703213A, NN705513D, NN706513A, NN706513B, NN706613A, NN706613B, NN708713A, NN708713B, NN711413A, NN711413B, NN713113A, NN713113B, NN713213C, NN713213D, NN714513B, NN714613C, NN716613A, NN719413B, NN719513C, NN720613B, NN720713A, NN724713B, NN724813A, NN726813A, NN726813B, NN726913A, NN728313A, NN728313B, NN729713A, NN729713B, NN730913C, NN730913D, NN732613B, NN733813B, NN733913A, NN735313A, NN735313B, NN801413D, NN801513A, NN802913A, NN804313A, NN804313B, NN805713B, NN805813A, NN809913B, NN811213D, NN812613D, NN812713A, NN814013C, NN814013D, NN815513A, NN816813D, NN816913A, NN819613C, NN819613D, NN822513A, NN822513B, NN826613C, NN826613D, NN826713A.",
      "center_classification_date": "20190117",
      "distribution_pattern": "Nationwide distribution AR, AZ, CA, CT, FL, HI, IA, ID, IL, KS, LA, MA, MD, MI, MN, MO, MS, NC, NH, NY, OH, PA, PR, RI, SC, TN, TX, UT, VA, VT, WA, WI.    International distribution to Canada.",
      "state": "WI",
      "product_description": "U by Kotex¿ Sleek¿, Regular/Super Tampons, 34 Count Multipack",
      "report_date": "20190123",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Kimberly-Clark Corporation",
      "recall_number": "Z-0750-2019",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "81759",
      "termination_date": "20210602",
      "more_code_info": "",
      "recall_initiation_date": "20181211",
      "postal_code": "54956-9317",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}