{
  "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,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "184623",
      "product_res_number": "Z-0781-2021",
      "event_date_initiated": "2020-11-13",
      "event_date_created": "2021-01-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2021-10-26",
      "res_event_number": "86826",
      "product_code": "OGR",
      "product_description": "Thyroid Pack CKHA-LF, Model DYNJ50352B - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.",
      "code_info": "Lot 20HBM370 (Expiration 02/28/2025); 20IBB678 (Expiration 03/31/2025); 20KBP338 (Expiration Date: 05/31/2025 never distributed)",
      "firm_fei_number": "1417592",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "3 Lakes Dr",
      "city": "Northfield",
      "state": "IL",
      "postal_code": "60093-2753",
      "additional_info_contact": "Kassandra Cotner\n866-359-1704",
      "reason_for_recall": "The cylindrical sponge component is not x-ray detectable.",
      "root_cause_description": "Process control",
      "action": "Customers were notified by email on 11/13/2020.  Customers are asked to return the response form via fax or email.  The recalling firm will send subsequent letters to consignees that have not provided a response to the recall notification within the allotted time.\n\nNo product is to be returned to Medline Industries.  Consignees are instructed to apply labels to their affected kits and return to inventory.  The label indicates that there is a recalled component within the pack, not to use it, and replace from a different sterile supply.  No other components within the kit are affected.",
      "product_quantity": "40",
      "distribution_pattern": "Foreign distribution only - Canada.",
      "openfda": {
        "device_name": "Ear, Nose, And Throat Surgical Tray",
        "medical_specialty_description": "Ear, Nose, Throat",
        "regulation_number": "874.4420",
        "device_class": "1",
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