TheraBand Kinesiology Tape 12745Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00087453127454), received between Nov 26, 2019 and Nov 26, 2019 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryNov 26, 2019Adverse Event Without Identified Device or Use Problem

  MY SKIN ON MY LEFT ARM WAS INJURED WHILE USING THERABAND KINESIOLOGY TAPE DISTRIBUTED BY (B)(4). I APPLIED THE TAPE AS INSTRUCTED AND SHOWN BY A MEDICAL PROFESSIONAL. THE TAPE STAYED ON MY ARM FOR 24 HOURS MUCH LESS THAN A MAXIMUM OF 5 DAYS. I NOTICED THAT MY ARM FELT DIFFERENT AND WHEN I TOUCHED THE AREA, MY SKIN WAS RAISED. I SLOWLY BEGAN REMOVING THE TAPE AND THERE WAS A BLISTER, REDNESS, A RASH, AND MY SKIN IRRITATED AND I WAS IN PAIN FOR DAYS FOLLOWING THE INJURY. BEFORE GOING TO THE DR, I WANTED TO GIVE IT A COUPLE OF DAYS TO SEE IF IT WOULD GET BETTER BY USING PURE SHEA BUTTER. I NURTURED THE INJURY FOR MORE THAN A WEEK AND THE BLISTER AND RASH HEALED. FDA SAFETY REPORT ID # (B)(4).

  Patient problems: Erythema; Pain; Rash; Skin Irritation; Swelling

  MAUDE report 9383541 ↗