{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Beachwood",
      "address_1": "23700 Mercantile Rd",
      "reason_for_recall": "The wiring may allow the lamps to turn on with the key switch rather than the timer.",
      "address_2": "",
      "product_quantity": "7 units",
      "code_info": "Serial numbers: 39870, 39873, 39874, 39866, 39867, 39871, 39869",
      "center_classification_date": "20170324",
      "distribution_pattern": "Worldwide distribution.  US states: IA, IL, MI, NY, PA, and WI.  Country: Jordan.    There are no government accounts for this recall.    There are no Canada accounts for this recall.    There are no Mexico accounts for this recall.",
      "state": "OH",
      "product_description": "Hand Foot II, UVB-138.  One device per box; device is surrounded by foam inserts inside a corrugated box.  For UV phototherapy treatment.",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "National Biological Corp",
      "recall_number": "Z-1683-2017",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "76725",
      "termination_date": "20190208",
      "more_code_info": "",
      "recall_initiation_date": "20170127",
      "postal_code": "44122-5900",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}