{
  "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": "97154",
      "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": "Letter",
      "distribution_pattern": "Distributed domestically to California, Florida, Pennsylvania, and Texas. No international distribution.",
      "recall_number": "Z-2156-2025",
      "product_description": "Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as:    C-SECTION PREP, REF DYNJ32702B",
      "product_quantity": "48 units",
      "reason_for_recall": "Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.",
      "recall_initiation_date": "20250612",
      "center_classification_date": "20250721",
      "report_date": "20250730",
      "code_info": "UDI/DI 10193489431070 (EA), 40193489431071 (CASE), Lot Numbers:  24EBR761"
    }
  ]
}