{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Woburn",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92187",
      "recalling_firm": "Cytrellis Biosystems, Inc.",
      "address_1": "299 Washington St Ste C",
      "address_2": "N/A",
      "postal_code": "01801-2793",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-1648-2023",
      "product_description": "Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring System System intended for the treatment of moderate and severe wrinkles in the mid and lower face.  Model #: Gen 4",
      "product_quantity": "89 units",
      "reason_for_recall": "Irregular core patterns could cause potential overlap of cores at the 8% setting, potentially leading to prolonged healing, irregularities in patient skin texture post-treatment, and/or scarring.",
      "recall_initiation_date": "20230407",
      "center_classification_date": "20230526",
      "report_date": "20230607",
      "code_info": "UDI-DI: B933ELCON010 All serial numbers"
    }
  ]
}