{
  "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": {
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  "results": [
    {
      "cfres_id": "64646",
      "product_res_number": "Z-0144-2008",
      "event_date_initiated": "2007-08-17",
      "event_date_posted": "2007-11-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-02-29",
      "res_event_number": "44957",
      "product_code": "HIG",
      "product_description": "Storz Equipment, Fluid Management Stand, for Fluid Management Systems, Product Number 26601EQ-KT",
      "code_info": "Product Number 26601EQ-KT (device has no lot or serial numbers)",
      "firm_fei_number": "2020550",
      "recalling_firm": "Karl Storz Endoscopy America Inc",
      "address_1": "600 Corporate Pointe",
      "city": "Culver City",
      "state": "CA",
      "postal_code": "90230-7600",
      "additional_info_contact": "Emily Cuadros\n800-421-0837 Ext. 4289",
      "reason_for_recall": "Outflow Difference: The accuracy of the Equimat displayed value could be influenced by external factors of the cart/stand and may result in a fluctuating or inaccurate reading.",
      "root_cause_description": "Device Design",
      "action": "All affected customers were notified via a Customer Letter issued on September 10, 2007 via FedEx overnight mail. The letter describes the problem with the device and the health hazard risk, and provides instructions for users to return the old stand and make arrangements for replacement stands.",
      "product_quantity": "287",
      "distribution_pattern": "Nationwide",
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