{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Bedford",
      "address_1": "28 Crosby Dr",
      "reason_for_recall": "Implant kit mislabeled",
      "address_2": "",
      "product_quantity": "2 units",
      "code_info": "Serial numbers: 0398482 & 0399917  Expiration Date: 12/31/2017",
      "center_classification_date": "20180213",
      "distribution_pattern": "US Distribution to the states of  :CA and TX.",
      "state": "MA",
      "product_description": "Total Knee Replacement , Catalog/Model # TPS-111-1111, UDI: +M572TPS1111111021/$$+31712310398482- and +M572TPS1111111021/$$+31712310399917/    Intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot be solely addressed by the use of a prosthetic device that treats only one or two of the three knee compartments, such as a unicondylar, patellofemoral, or bicompartmental prosthesis.",
      "report_date": "20180221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ConforMIS, Inc.",
      "recall_number": "Z-0600-2018",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "78902",
      "termination_date": "20190201",
      "more_code_info": "",
      "recall_initiation_date": "20170724",
      "postal_code": "01730-1402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}