{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83962",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed nationwide.",
      "recall_number": "Z-0299-2020",
      "product_description": "Trabecular Metal Reverse Shoulder System, Item Nos. 00434210613  00430900103  00434210613  00434210813  00434210817  00434210913  00434211013  00434211017  00434211113  00434211213  00434211217  00434211313  00434211413  00434211417  00434211513  00434211613  00434211713  00434211813  00434810613  00434810813  00434810817  00434810913  00434811013  00434811017  00434811113  00434811213  00434811217  00434811313  00434811413  00434811417  00434811513  00434811613  00434811713  00434811813  00434900813  00434900817  00434901013  00434901017  00434901213  00434901217  00434901413  00434903700  00434903811  00434903909  00434903912  32855090339  32855090353  32855090368  32855090375  32855090395  32855090512  32855090519  32855090520  32855090531  32855090585  32855090593  32855090598  32855090599  32855090628  32855090636  32855090637  32855090640  32855090658  32855090659  32855090734  47430703100  47430704100  47430706100",
      "product_quantity": "5,459,583 total devices",
      "reason_for_recall": "Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).",
      "recall_initiation_date": "20191010",
      "center_classification_date": "20191107",
      "termination_date": "20200519",
      "report_date": "20191113",
      "code_info": "All product manufactured prior to January 2014."
    }
  ]
}