{
  "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",
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      "address_1": "1023 Cherry Rd",
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      "postal_code": "38117-5423",
      "additional_info_contact": "Meghan Wells\n901-201-9298",
      "reason_for_recall": "The tibial tray lock detail is oversized (larger than specification).",
      "root_cause_description": "Device Design",
      "action": "Stryker notified consignees on about 09/30/2022, via letter that was hand delivered or sent via email titled, \"URGENT: MEDICAL DEVICE RECALL.\"  The letter instructed consignees to check inventory and quarantine any affected product, return the enclosed response form, arrange for the return of affected product and notify all applicable parties of the recall if product was further distributed.",
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