{
  "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": "Possible commingle of 13 MM and 14 MM  Intramedullary Bone Saw Cam Assembly -an Intramedullary Bone Saw Cam Assembly was labeled and etched as a 14 MM but measured as a 13 MM cam",
      "address_2": "",
      "product_quantity": "34 units",
      "code_info": "Lot Numbers: 334360, 366680, 366670  UDI:   (01)00880304386587(17)280805(10)334360  (01)00880304386587(17)280530(10)366680  (01)00880304386587(17)280530(10)366670",
      "center_classification_date": "20191203",
      "distribution_pattern": "Distribution to US states of CA, FL, IN, MN, MO, NY, and UT,  Australia, and New Zealand",
      "state": "IN",
      "product_description": "Biomet Orthopedics Intramedullary Bone Saw Cam Assembly  14MM-  Orthopedic manual surgical instrument  Item Number: 475665",
      "report_date": "20191211",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0595-2020",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "84224",
      "termination_date": "20200430",
      "more_code_info": "",
      "recall_initiation_date": "20191025",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}