{
  "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": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.",
      "address_2": "",
      "product_quantity": "219988 units (total)",
      "code_info": "664030",
      "center_classification_date": "20191122",
      "distribution_pattern": "US Nationwide distribution and countries of Argentina, Australia, Brazil, Canada, Chile, Colombia, Costa Rica, Ecuador, El Salvador, Italy, Netherlands, India, Japan, Korea, Malaysia, Mexico, New Zealand, Panama, Singapore, Taiwan, Thailand, Trinidad and Tobago, and Venezuela.",
      "state": "IN",
      "product_description": "HENNESSY LEFT CONST GLENOID HA, Item No. PM555360  UDI (01)00880304819597(17)260425(10)664030    Product Usage: Constrained Shoulder.",
      "report_date": "20191204",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0522-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83783",
      "termination_date": "20210721",
      "more_code_info": "",
      "recall_initiation_date": "20190821",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}