{
  "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": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65413",
      "recalling_firm": "Zimmer, Inc.",
      "address_1": "345 E Main St",
      "address_2": "N/A",
      "postal_code": "46580-2746",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the country of Japan.",
      "recall_number": "Z-1998-2013",
      "product_description": "00597001101                  Femur                   CR PRECOAT FEM COMP SIZE AML,  Rx, Sterile;     00597001102                  Femur                   CR PRECOAT FEM COMP SIZE AMR,  Rx, Sterile;     00597001201                  Femur                   CR PRECOAT FEM COMP SIZE BML,  Rx, Sterile;     00597001202                  Femur                   CR PRECOAT FEM COMP SIZE BMR,  Rx, Sterile.    Used in total knee arthroplasty and indicated for patients with severe pain.",
      "product_quantity": "192,355 all devices",
      "reason_for_recall": "Surgeons are implanting components of the NexGen Cruciate Retaining (CR) Complete Knee System in combinations that are not approved (micro with standard). Includes CR Micro Femurs, Articular Surface, Patellae, instruments and provisionals combined with standard components. A March 2012 recall reiterated the proper combination labeling, but the mis match problem continues.  Zimmer is removing the d",
      "recall_initiation_date": "20130607",
      "center_classification_date": "20130822",
      "termination_date": "20141215",
      "report_date": "20130828",
      "code_info": "REF 00597001101, all codes"
    }
  ]
}