Hearing Loss Products and Services
Advertise on Hearing Loss Web
Search This Site or the Web

Free Email Newsletter

Jobs, Jobs, Jobs

Hearing Loss Web Banner
Discussion Forum
Hearing Loss Events
Last Update: Nov 21

 

Home

About Us

Search

New to Hearing Loss?
In the News

Discussion Forum

HOH-LD-News

Advertise

Contact Us

Glossary

Events

 

Issues

Access

Oral Communications

Emergency Planning

Employment

Family

Hearing Aid Affordability

Identity

Law Enforcement

Psychological

Services

 

Medical

Audiology

Causes

Cures

Meniere's Disease

Tinnitus

Local Resources and Events
 
Employment Opportunities
 
Education Opportunities
 

Hearing Loss Products and Services

Advocates and Legal
Alerting Devices
Assistive Listening Devices
Business Services

Captioning

Financial Services
General Stores

Government

Health Products and Services
Hearing Aids
Hearing Aid Accessories
Hearing Aid Batteries
Hearing Aid Maintenance
Hearing Aid Repair
Hearing Dogs
Hearing Loss Organizations
Hints and Tips
Kids' Stuff
Medical Products and Services
Pagers

Publications

Relay Service
Sign Language Materials
Telecommunications Distribution Program

Telephones

Travel

TTYs (TDDs)

TTY Repairs

Two-Way Pagers

Technology

Alerting Devices

Assistive Listening Devices

Cochlear Implants

Hearing Aids

Speech Recognition

Telephones

Two Way Pagers

TTYs (TDDs)

Visual Communications

Links

Advanced Bionics Recalls Cochlear Implants

Editor: You've probably heard that Advanced Bionics has recalled several hundred cochlear implants, because of possible moisture contamination. Here's a notice from AB with additional information.

~~~~~~~~~~~~~~~~~~~

September 27, 2004

Dear Clinicians:

Advanced Bionics is asking you to return, immediately, all unused Advanced Bionics implantable cochlear stimulators: the CLARION(r) 1.2, the CLARION(r) CII, and the HiResTM90K. The recall arises from our concern about the possible presence of residual moisture in, or a potential loss of hermeticity of, the implantable cochlear stimulators. This recall is being made with the knowledge of the United States Food and Drug Administration.

Advanced Bionics has conducted a review of the reliability rates and failure modes of these products, which has led to this action. We would like to share the results and our decisions.

a.. The CLARION(r) 1.2, the oldest of the three models, is still in use by 92.0% of the recipients after 5 years. The CLARION(r) CII remains in 97.7% of patients after 3 years. While some of these devices have been removed for medical reasons (such as infection), most simply stopped working. Our investigation into these failures indicates that the most common cause was moisture in the stimulator that resulted in a premature loss of function.

b.. The HiResTM90K, our newest model, has had an explant rate of 1.1% at 12 months. Roughly half of these have been for medical reasons. Our investigations of the failures indicate that, in at least one instance, a significant cause was unexplained moisture on the internal circuitry. We have also found some residual moisture in other units that were hermetically sealed, although we have not yet determined whether these devices were affected by the moisture.

c.. Advanced Bionics is taking additional steps to reduce and control moisture levels in new units of the HiResT90K cochlear stimulator. We do not know how long this process will take, but until it is completed, we will not be able to supply cochlear implants. Please be assured that we are working on these improvements as quickly as possible. If you have a candidate scheduled for cochlear implant surgery, we recommend that you use a cochlear implant from another manufacturer or postpone implant surgery. We regret the inconvenience this interruption will cause you and your patients.

In addition, Advanced Bionics will soon be writing each cochlear implant user about the possibility of premature failure. Your patients may contact you with questions or for counseling, so we wanted you to be aware of the information in our letter before it is sent to users. They will be told that the signs and symptoms of failure are a sudden sensation of discomfort or pain, a sudden loud noise or popping sound, an intermittent functioning, a complete loss of sound, and in children, an unwillingness to wear the external headpiece. They will be advised that, if they experience any of these signs or symptoms, they should first try the backup cable, then the backup headpiece (if separate), and then the backup sound processor. If the signs or symptoms persist, they will be advised to remove the headpiece and contact their hearing care providers. They will be told that hearing clinics have a simple and quick way to test whether the implanted cochlear stimulator is fully functional.

If you have any questions regarding this letter, please call the Advanced Bionics implant hotline at 1-877-454-5038 between the hours of 5 AM and 5 PM Pacific Time, Monday through Friday.

Centers that we have shipped devices to, but where the implant registrations are outstanding, will receive a list of those devices with the serial number and shipment date. The document will be sent no later than September 28, 2004, close of business and will provide the information on how to return the products. It is important that the device registration and the product return be handled expeditiously.

Thank you in advance for your cooperation on this matter and we apologize for the inconvenience.

Sincerely,

Jeffrey H. Greiner
President and Co-Chief Executive Officer