{
  "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,
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  },
  "results": [
    {
      "cfres_id": "48888",
      "product_res_number": "Z-0116-2007",
      "event_date_initiated": "2005-04-28",
      "event_date_posted": "2006-10-28",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-02-21",
      "res_event_number": "36548",
      "product_code": "HJN",
      "product_description": "Venoscope Neonatal Transilluminator, Model NT01",
      "code_info": "The product is not lot coded on the exterior of the device and could not be identified by the consignee without disassembling the device to find the lack of an identifying mark.",
      "firm_fei_number": "1000306918",
      "recalling_firm": "Venoscope LLC",
      "address_1": "1018 Harding Street",
      "address_2": "Suite 104",
      "city": "Lafayette",
      "state": "LA",
      "postal_code": "70503",
      "additional_info_contact": "Frank Creaghan\n800-294-7655",
      "reason_for_recall": "Excessive heating due to incorrect wire assembly process.",
      "root_cause_description": "Other",
      "action": "The firm notified its consignees about the problem beginning on 04/28/2006 and requested the consignee (nurses and distributors) open the battery compartment and check for the absence of an identifying mark (there are no exterior lot numbers).  The recalling firm requested the return of all lights which had no identifying marks inside the battery compartment.",
      "product_quantity": "118 distributed",
      "distribution_pattern": "Nationwide",
      "openfda": {
        "registration_number": [
          "3011497859",
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        "fei_number": [
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        "k_number": [
          "K941035",
          "K912747",
          "K901309"
        ],
        "device_name": "Transilluminator, Battery-Powered",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.1945",
        "device_class": "1"
      }
    }
  ]
}