{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Raynham",
      "address_1": "325 Paramount Drive",
      "reason_for_recall": "Codman Certas Programmable Valves used for hydrocephalus may not operate properly",
      "address_2": "",
      "product_quantity": "369 units",
      "code_info": "Lot Codes:   CMBC2Y  CMDCN9  CMJC48  CMLC6D  CNCCLB  CNCCZ4  CNDBRG  CNDCNB  CNHC8M  CNJC4P  CNKCL4  CNLCL1  CNMB8Y  CNMDM0  CNNDHY  CNPCLZ  CPBC99  CPCC27  CPDBYJ  CMNBFF  CMNCDY  CNCB6M  CPBCRZ  CPDCKL",
      "center_classification_date": "20140128",
      "distribution_pattern": "Worldwide Distribution - US Nationwide, Australia, Austria, Belgium, Brazil, Switzerland, Czech Republic, Germany, Spain, Finland, France, Great Britain, Israel, Italy, Netherlands, Norway, Portugal, Russia, Saudi Arabia, Sweden, Slovenia, Slovakia, Turkey, South Africa, and UK.",
      "state": "MA",
      "product_description": "Codman Certas Programmable Valve In Line Valve with SiphonGuard Device, Catheter and Accessories  Product Code: 82-8805    Product Usage:  The CODMAN CERTAS Programmable Valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid) for the management of hydrocephalus. The valve can be set to a choice of eight opening pressure settings for constant intraventricular perssure drainage of CSF. The CODMAN CERTAS Therapy Management System (TMS) allows the non-invasive reading or adjustment of the valve setting.",
      "report_date": "20140205",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Codman & Shurtleff, Inc.",
      "recall_number": "Z-0862-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65179",
      "termination_date": "20150602",
      "more_code_info": "",
      "recall_initiation_date": "20130516",
      "postal_code": "02767",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}