Recall Z-0864-2014

Codman & Shurtleff, Inc. · initiated May 16, 2013

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Codman Certas Programmable Valve In Line Valve with SiphonGuard Device, Unitized Bactiseal Catheter and Accessories Product Code: 82-8807 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.

Codes / lots: Lot Codes: CLPCNB CMBCPT CMCC2W CMDB6L CMDDJV CMKB24 CMLCKN CMMC3H CMNBZH CNCB6N CNCCLJ CNCCZ3 CNDB8C CNDBRJ CNGBK4 CNHCZR CNJB1G CNJC4T CNJCMR CNKBZD CNLBVM CNLBZC CNMBFL CNNDH1 CNMBFM CNMDNK CNPBRL CNPCLV CPBBGT CNCCLH CNCCZ2 CNDB69 CNDCV0 CPBCR3 CPCBHC CPCBHD CPDCC3 CMMCGV CNBB11 CPBCR4 CPCCMN CPDBYL

Reason for recall

Codman Certas Programmable Valves used for hydrocephalus may not operate properly

FDA-determined cause: Device Design

Action taken

Codman issued an Urgent Notice dated May 16, 2013, to all affected customers. The letter identifed the affected product, problem and actions to be taken. Mitigation instructions are provided and if not followed or are not successful, either issue could lead to symptoms associated with under- or over-drainage. Units not implanted are to be returned. A U.S Acknowledgement Form and fax are requested to be completed and faxed to: 1-888-943-4193, or e-mail the form to codman8894@stericycle.com. If you have any questions on concerns in regards to this recall, please contact your Codman Representative or Stericycle at 1-888-943-2395.

Details

Recall number
Z-0864-2014
Initiated
May 16, 2013
Posted by FDA
January 29, 2014
Terminated
June 2, 2015
Product code
JXG – Shunt, Central Nervous System And Components
Quantity
746 units
Distribution
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.
Recalling firm
Codman & Shurtleff, Inc., Raynham, MA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0858-2014 Class IICodman Certas Programmable Valve In Line Valve Only Product Code: 82-8800 Product Usage:…Codman Certas Programmable Valves used for hydrocephalus may not operate properly 05/16/2013Terminated
Z-0859-2014 Class IICodman Certas Programmable Valve In Line Valve with Catheter and Accessories Product…Codman Certas Programmable Valves used for hydrocephalus may not operate properly 05/16/2013Terminated
Z-0860-2014 Class IICodman Certas Programmable Valve In Line Valve with Unitized BactiSeal Catheter and…Codman Certas Programmable Valves used for hydrocephalus may not operate properly 05/16/2013Terminated
Z-0861-2014 Class IICodman Certas Programmable Valve In Line Valve only with SiphonGuard Device Product…Codman Certas Programmable Valves used for hydrocephalus may not operate properly 05/16/2013Terminated
Z-0862-2014 Class IICodman Certas Programmable Valve In Line Valve with SiphonGuard Device, Catheter and…Codman Certas Programmable Valves used for hydrocephalus may not operate properly 05/16/2013Terminated
Z-0863-2014 Class IICodman Certas Programmable Valve In Line Valve with Siphonguard, Unitized Catheter and…Codman Certas Programmable Valves used for hydrocephalus may not operate properly 05/16/2013Terminated