{
  "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": "2026-10-28",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99960",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of CA, TC, AU, AE.",
      "recall_number": "Z-0272-2027",
      "product_description": "MEDLINE medical convenience kits labeled as:  FETOSCOPY CDS-LF,  Medline Product Number/SKU CDS840215P",
      "product_quantity": "10 kits",
      "reason_for_recall": "Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.",
      "recall_initiation_date": "20260909",
      "center_classification_date": "20261022",
      "report_date": "20261028",
      "code_info": "UDI/DI 10198459142031 (each) 40198459142032 (case), Lot numbers:  CDS840215P",
      "more_code_info": ""
    }
  ]
}