{
  "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": "2026-08-27",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "176737",
      "product_res_number": "Z-0510-2020",
      "event_date_initiated": "2018-12-12",
      "event_date_created": "2019-11-21",
      "recall_status": "Terminated",
      "event_date_terminated": "2021-01-22",
      "res_event_number": "83909",
      "product_code": "FER",
      "k_numbers": [
        "K171701"
      ],
      "product_description": "GelPOINT Path Transanal Procedural Pack with Epix Electrosurgical L-Hook with Smoke Evacuation, 4x5.5cm and 5mm x 42cm\nREF TA211  \nProduct Usage: The GelPOINT Path Transanal Access Platform is indicated for multiple instrument or camera access through the anus to perform various diagnostic and/or therapeutic procedures by using additional instruments.",
      "code_info": "Model Number: TA211 Lot Numbers: 1342169 and 1340118",
      "firm_fei_number": "2027111",
      "recalling_firm": "Applied Medical Resources Corp",
      "address_1": "22872 Avenida Empresa",
      "city": "Rancho Santa Margarita",
      "state": "CA",
      "postal_code": "92688-2650",
      "additional_info_contact": "Lauren Contursi\n949-713-8000",
      "reason_for_recall": "Unintentional shifting of the tip insulation of the firm's electrosurgical probes.",
      "root_cause_description": "Device Design",
      "action": "On12/12/2018, the firm sent an \"URGENT; MEDICAL DEVICE RECALL\" notification to customers via UPS informing them that this voluntary recall is being conducted due to the possibility that the insulation near the device tip may unintentionally shift.  Customers are asked to:\n Check their inventory for recalled product.\n Complete the attached Recall Notification Confirmation Form to acknowledge the recall and indicate if their facility is returning or has already used units or kits from the lots listed.\no If no product is being returned, to please indicate that on the Recall Notification Confirmation Form.\n Provide a no-charge P.O. number if replacement units or kits are requested.\n If customer is a distributor, they are instructed to notify any facilities to which they distributed units or kits from the affected lots, and to have them complete the appropriate sections of the Recall Notification Confirmation Form.\n Return the completed Recall Notification Confirmation Form to Applied Medical by emailing it to recall60787748@appliedmedical.com or faxing it to 949-713-8871.\n Return affected product and a copy of the Recall Notification Confirmation Form to Applied Medical following the instructions provided.\n\nFor product return questions, please contact the Manager of Customer Relations, RGA Dept. at (949) 713-8622 or by email at kmitchell@appliedmedical.com.\n\nFor regulatory questions, to contact (949) 713-8767 or by email at lcontursi@appliedmedical.com.",
      "product_quantity": "39 units Domestically and 112 units Internationally",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution and countries of Belgium; Germany; Switzerland; Spain; Finland; France; Great Britain; Israel; India; Italy; Lebanon; Netherlands; and Portugal.",
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          "K020702",
          "K133687",
          "K242668",
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          "K861017",
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          "K110792",
          "K080132",
          "K121604",
          "K993738",
          "K921291",
          "K810227"
        ],
        "device_name": "Anoscope And Accessories",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.1500",
        "device_class": "2",
        "registration_number": [
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