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WiTouch Pro 11.1500Recalls & reported problems

Hollywog, LLC · WiTouch brand over the counter transcutaneous electrical nerve simulator to be used for temporary relief of pain associated with sore and aching muscles in the back due to strain from exercise or normal household and work activities and relief of pain of the upper and lower back associated with arthritis. · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00853096004021), received between Jul 10, 2018 and Jul 10, 2018 — classified as 1 injury.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Atrial Fibrillation1
  • Atrial Flutter1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 10, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    I PURCHASED THE DEVICE ON (B)(6) AND I EXPERIENCED ISSUES WITH MY AFIB SHORTLY AFTER THE FIRST USE OF THE DEVICE. I CONTACTED MY PRIMARY CARE PHYSICIAN AT THE (B)(6) TO SEE IF I CAN CONTINUE USING THE DEVICE. I WILL STOP USING THE DEVICE UNTIL MY DOCTOR TELLS ME IF I CAN CONTINUE USING THE DEVICE.

    Patient problems: Atrial Fibrillation; Atrial Flutter

    MAUDE report 7675654 ↗

Other Stimulator, Nerve, Transcutaneous, Over-The-Counter devices

All Stimulator, Nerve, Transcutaneous, Over-The-Counter devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.