{
  "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": "Menlo Park",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72500",
      "recalling_firm": "Ceterix Orthopedics, Inc.",
      "address_1": "959 Hamilton Ave",
      "address_2": "N/A",
      "postal_code": "94025-1431",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-0250-2016",
      "product_description": "NovoCut Suture Manager; Ceterix catalog number CTX-001.    General and Plastic Surgery: Intended for use in arthroscopic surgery.",
      "product_quantity": "1364 units",
      "reason_for_recall": "The NovoCut Suture Manager device may cut the suture during knot tensioning and this may cause the suture knot to unravel.",
      "recall_initiation_date": "20151013",
      "center_classification_date": "20151109",
      "termination_date": "20160212",
      "report_date": "20151118",
      "code_info": "Ceterix catalog number CTX-001;  Lot numbers: M150016  M150056  M150078  M150105  M150136  M150182  M150185  M150202  M150207  M150225  M150239."
    }
  ]
}