{
  "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": "2026-08-13",
    "results": {
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  "results": [
    {
      "cfres_id": "48702",
      "product_res_number": "Z-0182-2007",
      "event_date_initiated": "2006-08-29",
      "event_date_posted": "2006-11-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-07-26",
      "res_event_number": "36470",
      "product_code": "JOS",
      "k_numbers": [
        "K973234"
      ],
      "product_description": "MIDAS TOUCH Electrosurgical/102 mm (4 inch) Blade Electrodes, Disposable, Sterile Single Use Device, Part #30-0012 and #30-0002. The electrodes are individually packaged in Tyvek bags with 12 packages per case.",
      "code_info": "4 inch Standard Electrodes - Model Number: 30-0002, Lot Numbers:  110201, 116228, 117331, 117985, 120959 and 000501; and 4 inch Modified Electrodes - Part Number:  30-0012, Lot Numbers:  110101, 113523, 113877, 114428, 114527, 115294, 115420, 119874, 120223, 120732 and 120883.",
      "firm_fei_number": "3000719969",
      "recalling_firm": "Olsen Medical",
      "address_1": "3001 W Kentucky St",
      "city": "Louisville",
      "state": "KY",
      "postal_code": "40211-1505",
      "additional_info_contact": "502-772-4280",
      "reason_for_recall": "Testing conducted by the firm indicates that electrodes identified with certain part numbers may fall out from the electrosurgical pencil or handle presenting the potential for harm or injury to the patient and/or user.",
      "root_cause_description": "Other",
      "action": "The firm issued an ''Urgent: Device Recall'' notification to their customers via letter and E-mail on 8/29/2006 and 8/30/2006. The letter informs the customers of this problem and asks that the customers contact their sub-accounts and notify them of the problem if they have further distributed any of the suspect part numbers. The letter also asks that the distributor/customer(s) have the subaccounts discontinue use of the product; and return the held product to the distributor (who in turn, should return the product to Olsen Medical for reimbursement).  The customers are asked to complete and fax back to the recalling firm, an attached Acknowledgement form documenting receipt of the recall notification by the customer/employee with name and date received. The firm also asked that the customer supply information regarding the amount of inventory /shipped on a checklist. The amounts received are broken down on the Checklist by Lot Number with the amount of product in inventory  and the amount of product shipped. These amounts are reported by the responders by ''pieces and cases'' on hand at the time that the notice was received.",
      "product_quantity": "81 cases/972 pieces",
      "distribution_pattern": "Worldwide, including USA, Japan, and New Zealand.",
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        "device_name": "Electrode, Electrosurgical",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4400",
        "device_class": "2"
      }
    }
  ]
}