{
  "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": "2026-03-18",
    "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": "90946",
      "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": "N/A",
      "distribution_pattern": "US Nationwide distribution in the states of CA, MN, NC, NY, OK, PA, TN, TX.",
      "recall_number": "Z-0166-2023",
      "product_description": "MEDLINE CVC BARRIER KIT, REF DYNJ80485.  Convenience kit used in medical procedures.",
      "product_quantity": "50 kits",
      "reason_for_recall": "Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.",
      "recall_initiation_date": "20220930",
      "center_classification_date": "20221101",
      "report_date": "20221109",
      "code_info": "UDI/DI (01) 40195327045471, Lot Number 22ABT774"
    }
  ]
}