{
  "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  672009100  672009101  672009103  672009200  672009203  672011101  672011103  672011200  672011201  672011203  672013100  672013101  672013103  672013200  672013203  672016101  672016103  672016200  672016203  672019100  672019101  672019200  672019201  672022101  672022103  672022200  672022201  672025100  672025200",
      "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 Constrained Knee System  NKII CCK TIB INS SZ00/0-L  NKII CCK TIB INS SZ1/2-LF  NKII CCK TIB INS SZ3-5 -L  NKII CCK TIB INS SZ00/0-R  NKII CCK TIB INS SZ3-5 -R  NKII CCK TIB INS SZ1/2-LF  NKII CCK TIB INS SZ3-5 -L  NKII CCK TIB INS SZ00/0-R  NKII CCK TIB INS SZ1/2-RT  NKII CCK TIB INS SZ3-5 -R  NKII CCK TIB INS SZ00/0-L  NKII CCK TIB INS SZ1/2-LF  NKII CCK TIB INS SZ3-5 -L  NKII CCK TIB INS SZ00/0-R  NKII CCK TIB INS SZ3-5 -R  NKII CCK TIB INS SZ1/2-LF  NKII CCK TIB INS SZ3-5 -L  NKII CCK TIB INS SZ00/0-R  NKII CCK TIB INS SZ3-5 -R  NKII CCK TIB INS SZ00/0-L  NKII CCK TIB INS SZ1/2-LF  NKII CCK TIB INS SZ00/0-R  NKII CCK TIB INS SZ1/2-RT  NKII CCK TIB INS SZ1/2-LF  NKII CCK TIB INS SZ3-5 -L  NKII CCK TIB INS SZ00/0-R  NKII CCK TIB INS SZ1/2-RT  NKII CCK TIB INS SZ00/0-L  NKII CCK TIB INS SZ00/0-R",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-1256-2014",
      "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"
    }
  ]
}