{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "cfres_id": "42771",
      "product_res_number": "Z-0270-06",
      "event_date_initiated": "2005-10-31",
      "event_date_posted": "2005-12-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-06-07",
      "res_event_number": "33945",
      "product_code": "FGY",
      "product_description": "Fusion OMNI- GT * DOME TIP: ERCP Catheter: 6.0 FR./200 CM. 8 Minimum Accessory Channel: 4.2 MM * Disposable  Single Use Only * Compatible Wire Guide: .035'' * Rx Only * Wilson-Cook Medical * GI Endoscope * 4900 Betharine Station * Winston-Salem, NC 27105",
      "code_info": "Lot number: W2073307, W2073308, W2074626, W2074627, W2074628, W2074629, W2074630, W2075126, W2075127, W2075128, W2075129, W2075130, W2076301, W2076302, W2076303, W2076304, W2076305, W2076306, W2076843, W2076844, W2076845, W2076846, W2076847, W2076848, W2076849, W2076850, W2076851, W2076852, W2076853, W2076854, W2076855, W2076856, W2076857, W2101351, W2103706, W2104274, W2104275, W2108267, W2108774, W2109312, W2109313, W2111333, W2114602, W2114603, W2116350, W2118471, W2121588, W2121589, W2122051, W2122052, W2122053, W2124537, W2125592, W2125593, W2125594, W2125595, W2129956, W2125597, W2129958",
      "firm_fei_number": "1037905",
      "recalling_firm": "Wilson-Cook Medical Inc",
      "address_1": "5951 Grassy Creek Blvd",
      "city": "Winston Salem",
      "state": "NC",
      "postal_code": "27105-1206",
      "additional_info_contact": "Sharon Miles\n336-744-0157 Ext. 6325",
      "reason_for_recall": "Misbranded; The catheter size listed on the product label is 6 French, which is inaccurate. The catheter size is more accurately described as 7 French.",
      "root_cause_description": "Other",
      "action": "Consignees were notified by letter on/about 11/04/2005.",
      "product_quantity": "1045 units",
      "distribution_pattern": "Nationwide, Argentina, Australia, Bahamas, Bolivia, Canada, Chile, Columbia, Costa Rica, Dominican Republic, Denmark, Ecuador, Egypt, El Salvador, Guatemala, Holland, Hong Kong, India, Ireland, Israel, Korea, Malaysia, New Zealand, Peru, Puerto Rico, Singapore, Taiwan, Uruguay, Venezuela, and West Indies.",
      "openfda": {
        "k_number": [
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        "device_name": "Cannula, Injection",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4200",
        "device_class": "1",
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