{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Alton",
      "address_1": "620 East Third Street",
      "reason_for_recall": "The devices were not shipped with the Starter Kits.",
      "address_2": "",
      "product_quantity": "26 lasers",
      "code_info": "Serial Numbers: FLM4184, FLM2003, FLM3324, FLM1409, FLM2906, FLM2136, FLM4948, FLM3134, FLM4587, FLM3281, FLM2179, FLM1467, FLM1239, FLM3361, FLM3319, FLM3685, FLM2915, FLM1230, FLM3229, FLM4094, FLM4135, FLM4545, FLM4905, FLM3913, FLM1680, FLM1776",
      "center_classification_date": "20150115",
      "distribution_pattern": "US: Nationwide (AL, CA, FL, GA, IL, MN, MO, NC, ND, NH, NJ, NM, NY, PA, TX, VA, WA)",
      "state": "IL",
      "product_description": "Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries.",
      "report_date": "20150121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ziemer Usa Inc",
      "recall_number": "Z-0988-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70024",
      "termination_date": "20180220",
      "more_code_info": "",
      "recall_initiation_date": "20141218",
      "postal_code": "62002",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}