{
  "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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      "product_res_number": "Z-0276-2008",
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      "res_event_number": "45326",
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      "address_1": "345 E. Main St.",
      "city": "Warsaw",
      "state": "IN",
      "postal_code": "46580-2304",
      "additional_info_contact": "800-846-4637",
      "reason_for_recall": "Mislabeled as to size; 54mm package contains 46 mm device and vice versa.",
      "root_cause_description": "Packaging process control",
      "action": "Zimmer GmbH notified Distributors via a Product Recall Notification letter, dated 9/26/07, instructing them to return the products and to subrecall.",
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