{
  "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-0138-2016",
      "product_description": "ConForMIS iUni Unicondylar Knee Replacement System:    iUNI G2, Left Lateral  Catalog Number: M57220600230 (US)                                   M5722INT0600230  (OUS)",
      "product_quantity": "7 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):   0355239  0355108  0355474  0354538  Serial Numbers (OUS):   0353919  0354845  0354849"
    }
  ]
}