ARIA WIFI SMART SCALE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-07 for ARIA WIFI SMART SCALE manufactured by Fitbit Inc.

Event Text Entries

[132548013] I am not sure if this qualifies but there is a serious problem with fitbit watches. A couple months ago i was having random times where my nerve hurt right under my fitbit. That is the only way to explain it, it didn? T feel muscle or skeletal. It felt like nerves were hurting. Then i woke up in the middle of the night with my hand in a lot of pain, enough where i couldn't sleep. I took off the fitbit watch and the pain slowly subsided. I never had any problems with that type of pain until i started wearing the fitbit watch again a couple weeks ago. I slowly felt it creeping on again until last night i woke up in the middle of the night with the same pain that isn? T tolerable to sleep with. I took off the watch and will not wear it again. I looked through the fitbit forums and see literally hundreds of threads with hundreds of comments. Some of the threads seem a little exaggerated along with the comments, but if you look at the overall population, there is a lot of people who are having 'nerve type pain' while wearing the fitbit for long periods of time (and some short periods). The reason i feel like it is necessary for the fda or similar to step in is because, this not a onetime adverse event, this is hundreds of people complaining of a pain that fitbit's device is causing. Some people are not very intelligent and are doing things that could possibly harm them. People are switching the fitbit from hand to hand every day to get rid of the discomfort/pain. Others are just wearing it for a few days until it hurts and then removing it for a couple weeks. Also fitbit is very good at giving refunds or replacements at the drop of a hat. If you are getting very low complaints on this issue, that may be the cause. (which made me hesitate to contact you in the first place. However, i am an employee at a cgmp pharmaceutical manufacturer and now it is my duty to contact about ae's) the fitbit moderators commonly list that all watches are well below some type of electric radiation levels that is set by the fda. However i am concerned of a possibly low dose overlong period of time problem. I wore this fitbit (blaze) for a year until i started to get the discomfort. Again, i removed it for a couple of months and didn't have a problem. Put it back on, and a week or so, i am having the same discomfort. Is the product over-the-counter? Yes. Did the problem stop after the person reduced the dose or stopped taking or using the product? Yes. Did the problem return if the person started taking or using the product again? Yes. Date the person first started taking or using the product: (b)(6) 2017. Date the person stopped taking or using the product? (b)(6) 2018.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5082917
MDR Report Key8227809
Date Received2019-01-07
Date of Report2019-01-02
Date of Event2019-01-02
Date Added to Maude2019-01-08
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameARIA WIFI SMART SCALE
Generic NameANALYZER, BODY COMPOSITION
Product CodeMNW
Date Received2019-01-07
Device Availability*
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerFITBIT INC
Manufacturer Address2995 STEVEN MARTIN DRIVE FAIRFAX VA 22031 US 22031


Patients

Patient NumberTreatmentOutcomeDate
10 2019-01-07

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