{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Zuidland",
      "state": "",
      "country": "Netherlands",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94022",
      "recalling_firm": "D.O.R.C. Dutch Opthalmic Research Center Intl B.V.",
      "address_1": "Scheijdelveweg 2",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, CO, FL, IN, MD, NC, NY, OH, SC, TX and PR.",
      "recall_number": "Z-1332-2024",
      "product_description": "Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)",
      "product_quantity": "21 boxes x 6 units each = 126 units",
      "reason_for_recall": "When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the  laser fiber tip precisely.",
      "recall_initiation_date": "20240115",
      "center_classification_date": "20240321",
      "report_date": "20240327",
      "code_info": "Product Number: 7225.ALC; UDI/DI: 08717872014203; All lots starting with a number between 2470 and 18705.",
      "more_code_info": ""
    }
  ]
}