{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84753",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to AL  CA  FL  IA  IL  MD  MI  MN  MO  MS  NC  NE  NJ  NY  PA  TX  UT  VA  WA  WI",
      "recall_number": "Z-1347-2020",
      "product_description": "THP Hip Plating System, Item Nos. 14-451070  14-451075  14-451080  14-451085  14-451090  14-451095  14-451100  14-451105  14-451110  14-451115  14-451120  14-451125  14-451130  .    The product is a metallic bone fixation system.",
      "product_quantity": "1662",
      "reason_for_recall": "Potential increase in fracture rate was detected during internal testing, in addition to potential discoloration inside the inner pouch of the packaging.",
      "recall_initiation_date": "20200107",
      "center_classification_date": "20200224",
      "termination_date": "20210408",
      "report_date": "20200304",
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