{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "Zimmer Biomet is conducting a medical device recall for two lots of Comprehensive Humeral stems. The lots were commingled during the manufacturing process and were etched with incorrect lot numbers. The size difference between the two stem sizes is 1.1 inches. It is visually recognizable by the user that the box label does not match the contents of the box.",
      "address_2": "",
      "product_quantity": "12",
      "code_info": "PN: 113617, LN: 552850, UDI# - (01) 00880304554184 (17) 271014 (10) 552850",
      "center_classification_date": "20180313",
      "distribution_pattern": "US Nationwide in the states of MN, NJ, CA, TX, ND",
      "state": "IN",
      "product_description": "Humeral Stem 55mm(Size 13)    Product Usage:  Intended for primary and revision total shoulder arthroplasty as well as hemi-arthroplasty",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0980-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79385",
      "termination_date": "20180904",
      "more_code_info": "",
      "recall_initiation_date": "20171208",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}