ICYHOT SMART RELIEF TENS THERAPY Adverse Event — Malfunction (MDR MW5094268)

Name: ICYHOT SMART RELIEF TENS THERAPY Adverse Event — Malfunction (MDR MW5094268)
Creator: DeviceEvents

ICYHOT SMART RELIEF TENS THERAPY Adverse Event — Malfunction (MDR MW5094268) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ICYHOT SMART RELIEF TENS THERAPY; Generic name: STIMULATOR, NERVE, TRANSCUTANEOUS, OVER-THE-COUNTER; Manufacturer: CHATTEM / SANOFI US SERVICES INC..

Device	ICYHOT SMART RELIEF TENS THERAPY
Generic name	STIMULATOR, NERVE, TRANSCUTANEOUS, OVER-THE-COUNTER
Manufacturer	CHATTEM / SANOFI US SERVICES INC.
Report number	MW5094268
Event type	Malfunction
Product problem	Y
Date received	2020-04-24
Narrative	THE TENS UNIT DOESN'T WORK PROPERLY, AND IN RESEARCHING IT, THIS SEEMS TO BE A COMMON OCCURRENCE WITH THE ICYHOT SMART RELIEF SYSTEM. YOU ARE TO SNAP THE POWER UNIT ONTO ADHESIVE PAD, BUT WHILE ONE SNAPS AND GOES ON FINE, THE OTHER SIDE DOESN'T MATCH UP QUITE RIGHT SO YOU HAVE TO MOVE IT AROUND A LITTLE TO GET IT TO SNAP ON. THIS PUT A SMALL WRINKLE IN THE PAD BY BOTH SNAPS, VERY SLIGHTLY. WHEN YO
Source	openFDA MAUDE (device adverse events)

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