{
  "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  672509100  672509101  672509200  672509203  672511100  672511103  672513101  672513103  672513201  672516103  672519103  672522201  672525103  672525203",
      "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 Posterior Stabilized (P.S.) Condylar Tibial Inserts:  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS INS TIB SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ  N-K II CONS PS TIB INS SZ",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-1257-2014",
      "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"
    }
  ]
}