{
  "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": "409 units",
      "code_info": "Lot Codes:   CMJCMD  CMBC2Z  CMDB7C  CMJC49  CMBCPR  CMCC2T  CMDBHC  CMLBLZ  CMMB14  CNDBCY  CNDCV2  CNJCFT  CNKBH6  CNLB57  CNMDNL  CNNCWD  CNPB1Z  CPBB3J  CPBDBB  CPCCM0  CPDBYK",
      "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, Unitized Catheter and Accessories  Product Code: 82-8806      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-0863-2014",
      "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"
    }
  ]
}