{
  "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": "73142",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) and Internationally to   ARGENTINA               AUSTRALIA  AUSTRIA  BARBADOS  BELGIUM  BERMUDA  BOLIVIA  BRAZIL  CARIBBEAN  CHILE  CHINA  COLOMBIA  COST RICA  DENMARK  DOMINICAN REPUBLIC  DORAL FL  ECUADOR  EL SALVADOR  ENGLAND  FRANCE  GERMANY  GUATEMALA  HONDURAS  HONG KONG  INDIA  ISRAEL  ITALY  JAMAICA  JAPAN  KOREA  MALAYSIA  MEXICO  NEW ZEALAND  NICARAGUA  PANAMA  PERU  SINGAPORE  SPAIN  SWEDEN  SWITZERLAND  TAIWAN  THAILAND  VENEZUELA  WEST INDIES  Canary Islands  Croatia  Cyprus  Czech Republic  Canada",
      "recall_number": "Z-0843-2016",
      "product_description": "CPT 12/14 COCR  prosthesis, hip, semi-constrained, metal/polymer, porous uncemented  various sizes  The CPT Hip System is indicated for cemented use in:   Patients suffering from severe hip pain and disability due to rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, collagen disorders, avascular necrosis of the femoral head, and nonunion of previous fractures of the femur.   Patients with congenital hip dysplasia, protrusio acetabuli, or slipped capital femoral epiphysis.   Patients suffering from disability due to previous fusion.   Patients with previously failed endoprostheses and/or total hip components in the affected extremity.   Patients with acute femoral neck fractures.\"",
      "product_quantity": "289",
      "reason_for_recall": "LDPE bag containing the implant adheres to the highly polished implant surface.",
      "recall_initiation_date": "20160111",
      "center_classification_date": "20160222",
      "termination_date": "20170523",
      "report_date": "20160302",
      "code_info": "Item numbers:  00-8114-040-00  00-8114-050-00  Lot numbers:  61790499  61878931  61891348  61907682  61993208  61993210  62030932  62038367  62106796  62106797  62148557  62161479  62206538",
      "more_code_info": ""
    }
  ]
}