{
  "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": [
    {
      "country": "United States",
      "city": "Athens",
      "address_1": "1627 Enterprise St",
      "reason_for_recall": "The ML 7090 Calibrated LASIK Blade (CLB) will not fit into the AMO Amadeus Metal Blade Holder.",
      "address_2": "",
      "product_quantity": "360 units",
      "code_info": "Lot 1490288",
      "center_classification_date": "20150313",
      "distribution_pattern": "Distributed in the states of CA, AL, GA, and TN, and the countries of Chile and Germany.",
      "state": "TX",
      "product_description": "ML 7090 Calibrated LASIK Blade (CLB); CLB CALIBRATED LASIK BLADE 10.    ML 7090 Calibrated LASIK Blade (CLB) is to be used as replacement blades for the AMO Amadeus Microkeratome, to perform lamellar keratectomy procedures.",
      "report_date": "20150325",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Med-logics Inc",
      "recall_number": "Z-1268-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70348",
      "termination_date": "20151028",
      "more_code_info": "",
      "recall_initiation_date": "20150113",
      "postal_code": "75751-8839",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}