HCMA's Implantable device questionnaire
Do you have an implantable defibrillator or pacemaker?
Yes 41 Votes 82.0 %
No 9 Votes 18.0 %
Total 50 Votes

Have you ever had a recall or alert issues on your device?
Yes 30 Votes 60.0 %
No 17 Votes 34.0 %
I am not sure 3 Votes 6.0 %
Total 50 Votes

Have you ever had a recall or alert on your leads?
Yes 9 Votes 18.0 %
No 33 Votes 66.0 %
I am not sure 8 Votes 16.0 %
Total 50 Votes

If you answered yes to having been part of a recall or alert do you feel you recieved this information in a timely manner?
Yes 19 Votes 38.0 %
No 20 Votes 40.0 %
I am not sure 11 Votes 22.0 %
Total 50 Votes

Do you think the FDA is doing the best job they can in monitoring the device industry?
Yes 5 Votes 10.0 %
No 21 Votes 42.0 %
I am not sure 10 Votes 20.0 %
I do not know what oversight they have over the industry 14 Votes 28.0 %
Total 50 Votes

Do you think the device manufacturers are doing their best to inform patients in the event of a recall?
Yes 10 Votes 20.0 %
No 24 Votes 48.0 %
I am not sure 16 Votes 32.0 %
Total 50 Votes

If a device is recalled who should be responsible for the cost of replacement?
The manufacturer 42 Votes 84.0 %
The patients insurance company 0 Votes 0 %
The patient 0 Votes 0 %
It should be shared between the manufacturer and the insurance comapny based on the age of the device 8 Votes 16.0 %
Total 50 Votes

Should a device manufacturer be permitted to sell exsisting devices once they have discovered a flaw and redesigned and produced a new version?
Yes 8 Votes 16.0 %
No 36 Votes 72.0 %
I am not sure 6 Votes 12.0 %
Total 50 Votes

Please let us know who you are. (choose one)
I am the patient 43 Votes 86.0 %
My loved one is the patient 5 Votes 10.0 %
I am a health care provider 2 Votes 4.0 %
I work in the device industry 0 Votes 0 %
Total 50 Votes


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