{
  "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": "2026-07-08",
    "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": "94356",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "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 - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.",
      "recall_number": "Z-2706-2024",
      "product_description": "Medline medical procedure kits labeled as follows:    a) ENDO KIT, REF DYKE1410A",
      "product_quantity": "3400 units",
      "reason_for_recall": "A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.",
      "recall_initiation_date": "20240322",
      "center_classification_date": "20240822",
      "report_date": "20240828",
      "code_info": "a) REF DYKE1410A, UDI/DI 40193489269223 (case), 10193489269222 (unit), Lot Numbers:    22EBO806, 22GBW168, 22IBP461, 22LBC090, 22LBM513, 23BBP271, 23DBM055, 23EBQ913, 23GBI842, 23IBF978, 23KBK768",
      "more_code_info": ""
    }
  ]
}