{
  "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": "29897",
      "product_res_number": "Z-0048-04",
      "event_date_initiated": "2003-10-08",
      "event_date_posted": "2003-10-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-11-10",
      "res_event_number": "27449",
      "product_code": "FEG",
      "k_numbers": [
        "K900035"
      ],
      "product_description": "Brodmerkel Colon Decompression Set, CDSB-10, Catheter Diameter: 10 Fr. Catheter Length: 350 cm. Sideports: 10, Standard wire Guide: .035''/480 cm. Disposable  Single use only, Rx Only. Cook, Wilson-Cook Medicl GI Endoscopy, 4900 Bethania Station Road, Winston-Salem, NC 27105.",
      "code_info": "Catalog # CDSB-10, Lot #1589467",
      "firm_fei_number": "1037905",
      "recalling_firm": "Wilson-Cook Medical Inc",
      "address_1": "4900 Bethania Station Rd & 5951 Grassy Creek Blvd.",
      "city": "Winston-Salem",
      "state": "NC",
      "postal_code": "27105",
      "additional_info_contact": "Jessica Hughes\n336-744-0157",
      "reason_for_recall": "Product may be packaged with an incorrect instructions for use (IFU) booklet.",
      "root_cause_description": "Other",
      "action": "Recall notification was sent via email to Wilson-Cook, sales representatives on 10/08/2003 for personal delivery to the affected accounts. Consignees were advised to quarantine and return all affected product via Federal Express (using Wilson-Cook Medical account) to the recalling firm. A verification form was included at the bottom portion of the notice to be returned with the affected product or faxed to Wilson-Cook. Replacement product  or account credit will be provided upon receipt of any affected devices.",
      "product_quantity": "9 pieces",
      "distribution_pattern": "The product was distributed to Hospitals located in CA, NC, PA, and WI.",
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          "K771048",
          "K880850",
          "K921104",
          "K171619",
          "K040388",
          "K960176"
        ],
        "device_name": "Tube, Double Lumen For Intestinal Decompression And/Or Intubation",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.5980",
        "device_class": "2",
        "registration_number": [
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