{
  "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  682000016  682001011  682001016  682001022  682001030  682002011  682002013  682002016  682002022  682002030  682003016  682003022  682003025  682004013  682004016  682005011",
      "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": "Apollo\" Revision/Constrained Knee System:  SZ0-16MM AK CCK TIB INSER  SZ1-11MM AK CCK TIB INSER  SZ1-16MM AK CCK TIB INSER  SZ1-22MM AK CCK TIB INSER  SZ1-30MM AK CCK TIB INSER  SZ2-11MM AK CCK TIB INSER  SZ2-13MM AK CCK TIB INSER  SZ2-16MM AK CCK TIB INSER  SZ2-22MM AK CCK TIB INSER  SZ2-30MM AK CCK TIB INSER  SZ3-16MM AK CCK TIB INSER  SZ3-22MM AK CCK TIB INSER  SZ3-25MM AK CCK TIB INSER  SZ4-13MM AK CCK TIB INSER  SZ4-16MM AK CCK TIB INSER  SZ5-11MM AK CCK TIB INSER",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-1261-2014",
      "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"
    }
  ]
}