{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "1800 W Center St",
      "reason_for_recall": "A complaint was received for a discolored All Poly Tibia. Root cause analysis found that the discoloration was the result of free radical oxidation. The  oxidation process was advanced prematurely as a result of the machined component being stored in a transparent container exposed to artificial  light for six years prior to inert packaging and sterilization of the device.",
      "address_2": "",
      "product_quantity": "3638 units",
      "code_info": "Item Number  621800809  621801809  621801819  621801913  621801916  621810816  621810909  621820809  621820811  621820911  621830811  621830909  621850916",
      "center_classification_date": "20140320",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including DC and the states of AK, AL, AR, AZ, CA, CO, CT, FL, IL, IN, KS, LA, ME, MI, MO, MS, NC, ND, NE, NJ, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, and WI, and the countries of   Canada, Australia, India, Austria, Japan, Czech Republic, Seoul Korea, France, Venezuela, Germany, Luxembourg, Spain, and Switzerland.",
      "state": "IN",
      "product_description": "Natural-Knee¿ II System:  POLY ULTRA TIB LT SZ00/9M  POLY ULTRA TIB LT SZ0/9MM  POLY ULTRA TIB LT SZ0/19M  POLY ULTRA TIB RT SZ0/13M  POLY ULTRA TIB RT SZ0/16M  ALL POLY ULTRA TIB LT SZ1  ALL POLY ULTRA TIB RT SZ1  ALL POLY ULTRA TIB LT SZ2  ALL POLY ULTRA TIB LT SZ2  ALL POLY ULTRA TIB RT SZ2  ALL POLY ULTRA TIB LT SZ3  ALL POLY ULTRA TIB RT SZ3  ALL POLY ULTRA TIB RT SZ5",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-1262-2014",
      "initial_firm_notification": "",
      "product_type": "Devices",
      "event_id": "67503",
      "termination_date": "20150324",
      "more_code_info": "",
      "recall_initiation_date": "20140225",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}