{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "29642",
      "product_res_number": "Z-0050-04",
      "event_date_initiated": "2003-09-15",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-10-21",
      "res_event_number": "27299",
      "product_code": "GWG",
      "product_description": "Channel Neuroendoscope, Standard Resolution, 13 cm, Catalog No. 2232-003.",
      "code_info": "A22148",
      "firm_fei_number": "3015531529",
      "recalling_firm": "Medtronic Neurosurgery",
      "address_1": "125 Cremona Drive",
      "city": "Goleta",
      "state": "CA",
      "postal_code": "93117",
      "additional_info_contact": "Jeffrey Henderson\n805-826-5603 Ext. 1770",
      "reason_for_recall": "Size mix-up. 13 cm product may be labeled as 21.6 mm and visaversa.",
      "root_cause_description": "Labeling mix-ups",
      "action": "Firm sales representatives will contact customers and hand deliver the recall notice.",
      "product_quantity": "10",
      "distribution_pattern": "TN, CO, GA and Japan",
      "openfda": {
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        "medical_specialty_description": "Neurology",
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}