{
  "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": "Fremont",
      "address_1": "47651 Westinghouse Dr",
      "reason_for_recall": "Laser aperture label was not affixed to device prior to shipment in the US.",
      "address_2": "",
      "product_quantity": "29 units (26 already re-labeled)",
      "code_info": "Part number: 173530U20  Serial numbers:  50010, 50127, 50136, 50277, 50310, 50311, 50330, 50331, 50357. 50358, 50359, 50382, 50383, 50408. 50417, 50418, 50426, 50439, 50445, 50446, 50471, 50514, 50552, 50558, 50573, 50600, 50610, 50611, 50651.",
      "center_classification_date": "20140730",
      "distribution_pattern": "Nationwide Distribution including IL NE NY, NH, CD, MI, TX, CA, PA, FL, KS, UT, MN, WI,. MO. and OR.",
      "state": "CA",
      "product_description": "MC-500 Multicolor Laser Photocoagulator; Distributed by NIDEK Inc.   Manufactured by NIDEK CO., Ltd, Japan.  For use in ophthalmic and retinal procedures.",
      "report_date": "20140806",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Nidek Inc",
      "recall_number": "Z-2132-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68766",
      "termination_date": "20141124",
      "more_code_info": "",
      "recall_initiation_date": "20140609",
      "postal_code": "94539-7474",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}