{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Sarasota",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71682",
      "recalling_firm": "ASO, LLC",
      "address_1": "300 Sarasota Center Blvd",
      "address_2": "N/A",
      "postal_code": "34240-9381",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Distribution to Rhode Island only",
      "recall_number": "Z-2460-2015",
      "product_description": "Carepak Sheer Adhesive Bandages 50 Sterile Bandages Assorted Sizes",
      "product_quantity": "655 cases.",
      "reason_for_recall": "Contain 0.1% Benzalkonium Chloride in the 5/8 bandages inside the assortment which is not listed as an active ingredient in the product label.",
      "recall_initiation_date": "20150610",
      "center_classification_date": "20150825",
      "termination_date": "20161012",
      "report_date": "20150902",
      "code_info": "Model  #141168; Lots #s 00013359, 00020722 and 00028721."
    }
  ]
}