{
  "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": "90911",
      "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": "Other",
      "distribution_pattern": "US Nationwide distribution in the state of California.",
      "recall_number": "Z-0120-2023",
      "product_description": "MEDLINE ADLT BLOOD CLUTURE COLLECT KIT, Reorder #:  DYNDH1245",
      "product_quantity": "900 kits",
      "reason_for_recall": "Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.",
      "recall_initiation_date": "20220909",
      "center_classification_date": "20221021",
      "report_date": "20221102",
      "code_info": "UDI/DI:  (01)40889942604723 (case), (01)10889942604722 (kit),Lot Number 22FMF306",
      "more_code_info": ""
    }
  ]
}