{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Lake Forest",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65098",
      "recalling_firm": "American Optisurgical Inc",
      "address_1": "26902 Vista Ter",
      "address_2": "N/A",
      "postal_code": "92630-8123",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution-USA (nationwide) including the states of AZ, CA, FL, GA, IL, KS, MA, MI, NC, NJ, OH, PA, TN, TX, VA, and WI.",
      "recall_number": "Z-1505-2013",
      "product_description": "FAST Procedure Kit.    Intended for use as a Minor Surgical Procedures Tray.",
      "product_quantity": "63 individual applicators",
      "reason_for_recall": "American Optisurgical, Inc initiated a recall of  ChloraPrep Hi-Lite Orange 3mL Applicator, in response to a sub-recall letter from Medline Industries, Inc due to lack of sterility assurance caused by an incomplete seal on the individual  unit packaging.",
      "recall_initiation_date": "20130430",
      "center_classification_date": "20130606",
      "termination_date": "20140324",
      "report_date": "20130612",
      "code_info": "Lot Numbers  07912-06  12912-04"
    }
  ]
}