{
  "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": "Mislabeled: incorrect serial number on the F4 A/P cut guide iJig.",
      "address_2": "",
      "product_quantity": "2 units",
      "code_info": "Serial Numbers: 0381024; 0381042  Exp Date: 2017-02-28",
      "center_classification_date": "20161125",
      "distribution_pattern": "Distributed to the states of CO and NV.",
      "state": "MA",
      "product_description": "ConforMIS iTotal Cruciate Retaining (CR) Knee Replacement System, Sterile  Catalog Number: TCR-111-1111.    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.",
      "report_date": "20161207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ConforMIS, Inc.",
      "recall_number": "Z-0658-2017",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "75553",
      "termination_date": "20161207",
      "more_code_info": "",
      "recall_initiation_date": "20161018",
      "postal_code": "01730-1402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}