{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98735",
      "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": "US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.",
      "recall_number": "Z-2148-2026",
      "product_description": "Medline medical convenience kits, containing Namic Manifold, Labeled as:  TAVI, Medline Kit Number/SKU DYNJ904981C",
      "product_quantity": "107 kits",
      "reason_for_recall": "Medline has identified the presence of particulate within the fluid path of the Manifolds.",
      "recall_initiation_date": "20260324",
      "center_classification_date": "20260508",
      "report_date": "20260520",
      "code_info": "UDI/DI each 10193489475135, UDI/DI case 40193489475136, Lot Numbers:  23GBR742, 23IBC951, 23JBM554, 23LBK506, 24BBO670, 24GBM624.",
      "more_code_info": ""
    }
  ]
}