{
  "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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      "event_date_initiated": "2009-09-04",
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      "res_event_number": "53434",
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      "address_1": "325 Corporate Drive",
      "city": "Mahwah",
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      "postal_code": "07430",
      "additional_info_contact": "RIchard Wolyn\n201-831-5158",
      "reason_for_recall": "Packaging mix up between the Taper V40 Femoral Head and the LFIT V40 Femoral Head.",
      "root_cause_description": "Process control",
      "action": "Stryker sent Notification letters and Product Accountability Forms via FedEx on September 4, 2009 with return receipt.  Corrected letters were sent on September 9, 2009.",
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