{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "51342",
      "product_res_number": "Z-0770-2007",
      "event_date_initiated": "2005-12-12",
      "event_date_posted": "2007-05-04",
      "recall_status": "Terminated",
      "event_date_terminated": "2013-02-20",
      "res_event_number": "37702",
      "product_code": "FEB",
      "k_numbers": [
        "K061430"
      ],
      "product_description": "83 plus Mini-flex with accessory crate, Custom Ultrasonics, Inc.",
      "code_info": "Serial numbers: 051305-J, 061705-E, 061605-F, and 061705-G.",
      "firm_fei_number": "2523209",
      "recalling_firm": "Custom Ultrasonics, Inc.",
      "address_1": "144 Railroad Dr",
      "city": "Ivyland",
      "state": "PA",
      "postal_code": "18974-1449",
      "additional_info_contact": "Frank Weber\n215-364-1477",
      "reason_for_recall": "The device was marketed without a 510k",
      "root_cause_description": "PMA",
      "action": "On 12/12/05, the recalling firm telephoned their sales representatives to inform them of the problem. Letter were hand delivered to the hospitals by the sales representatives.",
      "product_quantity": "4 units",
      "distribution_pattern": "Worldwide-The device was shipped to medical facilities in CA, GA, VA. and the UK.",
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        "device_name": "Accessories, Cleaning, For Endoscope",
        "medical_specialty_description": "Gastroenterology, Urology",
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        "device_class": "2",
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