{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "27512",
      "product_res_number": "Z-0017-04",
      "event_date_initiated": "2003-04-17",
      "event_date_posted": "2003-10-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-12-03",
      "res_event_number": "26326",
      "k_numbers": [
        "K000666"
      ],
      "product_description": "TC-PLUS Solution Tibial Component-- Symmetric",
      "code_info": "Lot 0211.13.4553",
      "firm_fei_number": "3002807898",
      "recalling_firm": "Plus Endoprothetik AG",
      "address_1": "Erlenstrasse 4b 4b erlenstrasse",
      "city": "Rotkreuz",
      "country": "Switzerland",
      "additional_info_contact": "Niel Delaney\n888-741-7587",
      "reason_for_recall": "Labeling/packaging mix-up.",
      "root_cause_description": "Other",
      "action": "Firm notified implanting surgeons by letter and telephone on   May 16, 2003 and on June 2, 2003.  One physician was contacted on August 26, 2003. The firm communicated the need to follow-up with the patients . Recall is complete.",
      "product_quantity": "15",
      "distribution_pattern": "TX, CA, VA, ID, NY, UT, FL",
      "openfda": {}
    }
  ]
}