{
  "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": {
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  "results": [
    {
      "cfres_id": "85822",
      "product_res_number": "Z-0263-2010",
      "event_date_initiated": "2009-10-05",
      "event_date_posted": "2009-11-16",
      "recall_status": "Terminated",
      "event_date_terminated": "2009-11-30",
      "res_event_number": "53549",
      "product_code": "DZI",
      "k_numbers": [
        "K040369"
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      "product_description": "Stryker Instruments 2.1 mm Cross-Cut Fissure Bur, carbide extended, sterile; REF 2296-101-621.",
      "code_info": "Lots 08311017 and 08336027.",
      "firm_fei_number": "1811755",
      "recalling_firm": "Stryker Instruments Div. of Stryker Corporation",
      "address_1": "4100 E. Milham Ave.",
      "city": "Kalamazoo",
      "state": "MI",
      "postal_code": "49001",
      "additional_info_contact": "269-323-7700 Ext. 3808",
      "reason_for_recall": "The cross-cuts are missing on the device, which will result in poor cutting and overheating and/or smoking of the device.",
      "root_cause_description": "Vendor change control",
      "action": "Consignees were notified by letter dated 10/5/09 and requested to return the devices to Stryker.  The international account was notified by email.",
      "product_quantity": "93",
      "distribution_pattern": "USA (California, Georgia, Louisiana, Ohio, Wisconsin) and Brazil.",
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