{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bryan",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99331",
      "recalling_firm": "Daavlin Distributing Company",
      "address_1": "205 W Bement St",
      "address_2": "",
      "postal_code": "43506-1264",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2742-2026",
      "product_description": "Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders",
      "product_quantity": "2 units",
      "reason_for_recall": "Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be \"4/5\" instead of \"7\" (counts were at ~1000 instead of ~5000).",
      "recall_initiation_date": "20260305",
      "center_classification_date": "20260715",
      "report_date": "20260722",
      "code_info": "Serial Numbers:  4-01440NB10CL, 2 4-01441NB10CL.",
      "more_code_info": ""
    }
  ]
}