{
  "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,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Sarasota",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91970",
      "recalling_firm": "ASO LLC",
      "address_1": "300 Sarasota Center Blvd",
      "address_2": "",
      "postal_code": "34240-9381",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution: IL. FL, CA, CT, OH, TX, IL, SC, and WI",
      "recall_number": "Z-1499-2023",
      "product_description": "WALGREENS BANDAGES, item number 196568, 110 CT VALUE PACK, 24 BOXES/MASTER (shipping container), Walgreens Family Pack ASSORTED BANDAGES, 110 ASSORTED SIZES (retail package)",
      "product_quantity": "919 cases of 24 units",
      "reason_for_recall": "The adhesive bandage contains 0.1% benzalkonium chloride impregnated in the pad and is not disclosed on the labeling.",
      "recall_initiation_date": "20230323",
      "center_classification_date": "20230502",
      "report_date": "20230510",
      "code_info": "UDI/DI 311917124506; Lot Numbers: 00176259, 00176260, 00176582.",
      "more_code_info": ""
    }
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}