{
  "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": "345 E Main St",
      "reason_for_recall": "This is an expansion of the June 2013 recall of NexGen Micro components.  Five (5) additional instruments have been identified that are associated only with the NexGen Micro components.  There is the potential for these devices to be inadvertently utilized during surgery, resulting in a delay.   The associated implants would not be available due to the previous recall.",
      "address_2": "",
      "product_quantity": "684 units",
      "code_info": "Part Number 00-5971-031-09",
      "center_classification_date": "20131206",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to Australia, Belgium, Canada, Denmark, Ecuador, Germany, India, Italy, Japan, Korea, Malaysia, Mexico, Netherlands, Peru, Singapore, South Africa, Spain, Switzerland, UAE, and UK.",
      "state": "IN",
      "product_description": "NexGen Complete Knee Solution  CR Articular Surface Provisional-Yellow 9mm Height Nonsterile    Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic loss of joint configuration, flexion deformities, and in revision of previous surgical attempts.",
      "report_date": "20131218",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-0462-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "66809",
      "termination_date": "20150506",
      "more_code_info": "",
      "recall_initiation_date": "20131119",
      "postal_code": "46580-2746",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}