FDA Adverse Event Injury Summary report: N

SONOLINE B (FETAL DOPPLER)

MDR report key: 8260724 · Received January 17, 2019

Report

Report Number
MW5083214
Event Type
Injury
Date Received
January 17, 2019
Date of Event
January 10, 2019
Report Date
January 15, 2019
Manufacturer
BABY DOPPLER / DAGAMMA INC.
Product Code
HGM
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
CA
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

I AM PREGNANT AND I AM AT WEEK (B)(6) OF MY PREGNANCY. I CAME ACROSS AN ADVERTISEMENT ON THE INTERNET ABOUT A DEVICE TO CHECK THE FETUS HEALTH AT HOME BY LISTENING TO THE BABY HEARTBEAT. I PURCHASED THE PRODUCT FROM A U.S SUPPLIER ON THE INTERNET AND RECEIVED IT IN 4 DAYS AT THE PRICE OF (B)(6). WE TRIED THE PRODUCT AT HOME AS PER INSTRUCTION IN THE BOX - I WAS NOT ABLE TO DETECT THE BABY HEARTBEAT, AND I TRIED THIS FOR OVER 20 MINUTES. THEN I FELT A BIT OF ANXIETY AS THE DEVICE PROBE (THE PART ON STOMACH WAS SOMEHOW HEALED.) THEN I STARTED SEARCHING THE NET AND FOUND A SHOCKING WARNING BY FDA TO AVOID USING THIS DEVICE AS THE OVERHEATING COULD POTENTIALLY HARM THE BABY ON THIS LINK: HTTPS://WWW.FDA.GOV /FORCONSUMERS/CONSUMERUPDATE/UCM095508.HTM; WE HAD TO GO IMMEDIATELY TO OUR DOCTOR AND SHE ALSO STRONGLY ADVISED AGAINST THE USE. I CONTACTED THE COMPANY WHICH WE BOUGHT THE PRODUCT (WWW.BABYDOPPLER.COM) ASKING FOR EXPLANATION. THEY MENTIONED THE PRODUCT IS NOT A MEDICAL UNIT, HOWEVER WHEN WE SEARCH ON FDA DATABASE, WE CLEARLY HAD LICENSED THIS PRODUCT UNDER THIS LICENSE K082480 AND THE DEVICE IS WITH PRESCRIPTION ONLY NOT OVER THE COUNTER. WE HAVE CONTACTED OUR FAMILY LAWYER TO SEE IF THIS CASE CAN BE LEGALLY PURSED. HE ADVISED US TO FILE A REPORT TO FDA TO HAVE A BACKUP FOR OUR CASE. THANKS FOR YOUR CONSIDERATION. (BABYDOPPLER.COM).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
52283 SONOLINE B (FETAL DOPPLER) MONITOR, ULTRASONIC FETAL HGM BABY DOPPLER / DAGAMMA INC. SONOLINE B

Patients

Seq Age Sex Outcome Treatment
1 32 YR Required Intervention