{
  "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",
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      "recall_status": "Terminated",
      "event_date_terminated": "2004-05-03",
      "res_event_number": "27690",
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      "product_description": "Stryker brand OrthoTec pulsed irrigation/suction handpiece and tubing set; part number 0203-020-000.",
      "code_info": "Lots 03082022, 03082042, 0308102, 03082122, 03082162, 03082202, 03082222, 03092242, 03092302, 03092322, 03092342, 03092402, 03092422, 03092442 and 03092462.",
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      "recalling_firm": "Stryker Instruments, Instruments Div.",
      "address_1": "4100 E. Milham",
      "city": "Kalamazoo",
      "state": "MI",
      "postal_code": "49001",
      "additional_info_contact": "Becky Ditty\n800-800-4236 Ext. 3434",
      "reason_for_recall": "Product sterility may have been compromised by an inadequate package seal.",
      "root_cause_description": "Other",
      "action": "Recall letters dated 11/12/03 were issued to each customer and sales representatives were requested to question each account about affected product.",
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