{
  "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-0837-2016",
      "product_description": "Gender PFJ FEMORAL COMP,   prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer  various sizes  \"  Osteoarthritis, traumatic arthritis, polyarthritis, and/or severe chondrocalcinosis of the patellofemoral joint.   The salvage of previously failed surgical attempts (e.g., arthroscopy, lateral release, cartilage transplantation).   History of patellar dislocation or patella fracture.   Dysplasia-induced degeneration. This device is intended for cemented use only.\"",
      "product_quantity": "5103",
      "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",
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}