{
  "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": "2026-04-15",
    "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": "81118",
      "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": "US Distribution to states of:: AR, KY, and WA.; Internationally  to: Australia and Japan.",
      "recall_number": "Z-0972-2019",
      "product_description": "Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 010000589     Biomet Comprehensive Reverse Shoulder products are indicated for use in patients whose shoulder joint has a grossly deficient rotator cuff with severe arthropathy and/or previously failed shoulder joint replacement with a grossly deficient rotator cuff.",
      "product_quantity": "52",
      "reason_for_recall": "The product was potentially being packaged without a taper adapter.",
      "recall_initiation_date": "20181221",
      "center_classification_date": "20190301",
      "termination_date": "20200506",
      "report_date": "20190313",
      "code_info": "Lot Numbers 994110, 921950  UDI Numbers:  (01) 0 0880304 53246 5 (17) 280920 (10) 994110  (01) 0 0880304 53246 5 (17) 280913 (10) 921950"
    }
  ]
}