{
  "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": "83099",
      "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": "The products were distributed US nationwide.    The products were distributed to the following foreign countries:  Argentina, Australia, Canada, Chile, China, Columbia, Costa Rica, Ecuador, India, Japan, Korea, Malaysia, Mexico, Netherlands, Thailand, Venezuela.",
      "recall_number": "Z-1960-2019",
      "product_description": "Comprehensive Reverse Shoulder Instrument Case  Outer (Outer Case Vault Only), Item Number 595509",
      "product_quantity": "92",
      "reason_for_recall": "Lack of an adequate sterilization validation.",
      "recall_initiation_date": "20190610",
      "center_classification_date": "20190712",
      "termination_date": "20200910",
      "report_date": "20190724",
      "code_info": "Lots: 262549  266083                          1441011  M642860       2881015  3021022  3081051  266083                          2591050                        2771027                        3231028                        MJ54320       MJ54330       MJ54350       MJ54340"
    }
  ]
}