{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "31872",
      "product_res_number": "Z-0357-04",
      "event_date_initiated": "2003-11-17",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-07-08",
      "res_event_number": "28434",
      "product_code": "--",
      "product_description": "Coherent brand Quattro Diode Laser Systems;\nA Quattro FAP System;\nModel Numbers/Serial Numbers: TFAP0004P--TFAP00048",
      "code_info": "Serial Numbers/Model Numbers: TFAP0004P--TFAP00048",
      "firm_fei_number": "2916213",
      "recalling_firm": "Coherent Inc Laser Group",
      "address_1": "5100 Patrick Henry Dr",
      "city": "Santa Clara",
      "state": "CA",
      "postal_code": "95054-1112",
      "additional_info_contact": "Scott H. Miller\n408-764-4594",
      "reason_for_recall": "Software problem that may cause the instrument to remain on and emitting laser radiation after the interlock has been activated.",
      "root_cause_description": "Other",
      "action": "On 11/7/03, all consignees were notified via Certified Mail and on-site visit by the firm''s sales representative, informing them of the affected devices and providing instructions on the recall.",
      "product_quantity": "52 units",
      "distribution_pattern": "52 units were released for distribution to consignees in U.S. nationally.",
      "openfda": {}
    }
  ]
}