{
  "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": "96163",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "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": "US:  CA",
      "recall_number": "Z-1173-2025",
      "product_description": "Medline RR-LIVER TRNS ACCESSORY PEDS, DUNJ63397;  medical procedure convenience kit",
      "product_quantity": "36 units",
      "reason_for_recall": "Medline is recalling medical convenience kits which were assembled with specific Coloplast Foley catheters and Prostatic catheters which were subsequently recalled due to a potential sterility issue detected during testing.",
      "recall_initiation_date": "20250103",
      "center_classification_date": "20250214",
      "report_date": "20250226",
      "code_info": "UDI/DI 10193489736755 (ea) 40193489736756 (cs), Lot Numbers:  22HLA247, 21HLA443, 21JLA520, 22GLA335."
    }
  ]
}