{
  "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": "San Marcos",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95290",
      "recalling_firm": "PACIFIC LASERTECH, LLC",
      "address_1": "215 Bingham Dr # 110",
      "address_2": "",
      "postal_code": "92069-1403",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-2975-2024",
      "product_description": "25-LHP-828, HeNe Laser System, 35 mW",
      "product_quantity": "4",
      "reason_for_recall": "These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control which requires,  Each laser system classified as a Class IIIb or IV laser product shall incorporate a key-actuated master control. The key shall be removable and the laser shall not be operable when the key is removed. , because while the laser is switched on, the key can be removed from the key switch.  The correction is replacement with a key switch that captures the key when in the on position.",
      "recall_initiation_date": "20240301",
      "center_classification_date": "20240910",
      "report_date": "20240918",
      "code_info": "25-LHP-828",
      "more_code_info": ""
    }
  ]
}