{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "31741",
      "product_res_number": "Z-0153-04",
      "event_date_initiated": "2003-09-12",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-04-29",
      "res_event_number": "28383",
      "product_code": "LS-99",
      "product_description": "Weber SolarJet S CO2 Vector Laser Coder System; Weber Marking Systems, Inc., Arlington Heights, IL 60005",
      "code_info": "serial number 09333451",
      "firm_fei_number": "1000298911",
      "recalling_firm": "Weber   Marking   System   Inc.",
      "address_1": "711 W Algonquin Rd",
      "city": "Arlington Heights",
      "state": "IL",
      "postal_code": "60005-4457",
      "additional_info_contact": "Mr. Chris Brown\n847-879-3404",
      "reason_for_recall": "The laser product failed to comply with the performance standards, including certification, identification, warning logotype label, aperture label and submission of a product report.",
      "root_cause_description": "Other",
      "action": "Recalled by letter dated 9/12/03.  The user account was advised of the labeling non-compliances and that a Weber Marking Systems representative would visit their location to correct the laser unit.",
      "product_quantity": "1 unit",
      "distribution_pattern": "Virginia",
      "openfda": {}
    }
  ]
}