{
  "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-0143-2016",
      "product_description": "ConForMIS iDuo Knee Bicompartmental Knee Replacement System , iDUO G2, Right Medial   Catalog Number: M57230600220 (US)                                  M5723INT0600220 (OUS)",
      "product_quantity": "12 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):  0354902, 0353696  Serial Numbers (OUS):  0349179  0352344  0352431  0352626  0353845  0353883  0353884  0354625  0355002  0355181"
    }
  ]
}