{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Austin",
      "address_1": "9800 Metric Blvd",
      "reason_for_recall": "U.S. Agent contacted Director Commercial Logistics, notifying him of incorrect color coded labels on two packages of e+tibial inserts.  There were 8 e+ tibial inserts of the same lot number in Finished Goods as the two from the agency. These devices were inspected and all were incorrectly labeled.",
      "address_2": "",
      "product_quantity": "5",
      "code_info": "Model/Catalog Number 391-15-708.  Lot/Serial Number 59602230.",
      "center_classification_date": "20130502",
      "distribution_pattern": "US Distribution to the state of California and International Distribution to the country of Venezuela.",
      "state": "TX",
      "product_description": "3DKnee e+ Tibial Insert. The insert is used along with the other components that comprise the 3DKnee System.",
      "report_date": "20130508",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Encore Medical, Lp",
      "recall_number": "Z-1213-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64859",
      "termination_date": "20130701",
      "more_code_info": "",
      "recall_initiation_date": "20130401",
      "postal_code": "78758",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}