{
  "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": "431 units",
      "code_info": "Lot Codes:   CLPCM9  CMBBB2  CMBBB3  CMDBHD  CMDCN7  CMDDJT  CMFBNK  CMFBNL  CMNBZG  CNDCP3  CNGBK5  CNHCZP  CNJB1F  CNJC4R  CNJCMP  CNKB0Y  CNLCL0  CNMCYY  CNMDNJ  CNNDH0  CNPBRK  CNPCLW  CPBBGR  CPCCBC  CPCCML  CPDCC2",
      "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 Unitized BactiSeal Catheter and Accessories  Product Code: 82-8803    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-0860-2014",
      "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"
    }
  ]
}