{
  "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,
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  "results": [
    {
      "cfres_id": "40284",
      "product_res_number": "Z-0366-06",
      "event_date_initiated": "2005-03-24",
      "event_date_posted": "2006-01-10",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-01-10",
      "res_event_number": "32533",
      "product_code": "HCA",
      "k_numbers": [
        "K853361",
        "K853362"
      ],
      "product_description": "7 cm Catheter Reservoir with 10 cm extension",
      "code_info": "M1330/PR07X/11-2009 and M1476/PR07X/12-2009",
      "firm_fei_number": "2518608",
      "recalling_firm": "Vygon Neuro",
      "address_1": "2495 General Armistead Ave",
      "city": "Norristown",
      "state": "PA",
      "postal_code": "19403-3685",
      "additional_info_contact": "Courtney Smith\n610-539-9300",
      "reason_for_recall": "stylet in package is shorter than that claimed on the label",
      "root_cause_description": "Other",
      "action": "The recalling firm issued a letter to their customers informing them of the problem and the need to return the product.",
      "product_quantity": "11 units",
      "distribution_pattern": "The product was shipped to a hospital in CA and a distributor in Germany.",
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        "device_name": "Catheter, Ventricular",
        "medical_specialty_description": "Neurology",
        "regulation_number": "882.4100",
        "device_class": "2"
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}