{
  "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": [
    {
      "status": "Terminated",
      "city": "Bedford",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72108",
      "recalling_firm": "ConforMIS, Inc.",
      "address_1": "28 Crosby Dr",
      "address_2": "N/A",
      "postal_code": "01730-1402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed Nationwide and in Germany, Switzerland, and UK.",
      "recall_number": "Z-0140-2016",
      "product_description": "ConForMIS iUNI Unicondylar Knee Replacement System   iUNI G2, Right Lateral  Catalog Number:  M57220600240 (US)                                   M5722INT0600240 (OUS)",
      "product_quantity": "6 units",
      "reason_for_recall": "May contain small amounts of ethylene glycol residue",
      "recall_initiation_date": "20150831",
      "center_classification_date": "20151021",
      "termination_date": "20160302",
      "report_date": "20151028",
      "code_info": "Serial Numbers (US):   0353697  0354749  0349417  0354328  Serial Number (OUS):  0352836  0355233"
    }
  ]
}