{
  "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  611001009  611001011  611001013  611002009  611002011  611002013  611003009  611003011  611003013",
      "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 - Unicompartmental Knee Prosthesis:  CONG TIB INS SZ1/2 9MM UN  CONG TIB INS SZ1/2 11MM U  CONG TIB INS SZ1/2 13MM U  CONG TIB INS SZ3/4 9MM UN  CONG TIB INS SZ3/4 11MM U  CONG TIB INS SZ3/4 13MM U  CONG TIB INS SZ 5/6 9MM U  CONG TIB INS SZ5/6 11MM U  CONG TIB INS SZ5/6 13MM U",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-1251-2014",
      "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"
    }
  ]
}