Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
iontoPATCH On-the-Go Patch Therapy Recalled by Tapemark Company Due to The dosage information on the pouch is incorrect;...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Tapemark Company directly.
Affected Products
iontoPATCH On-the-Go Patch Therapy, Transdermal Iontophoretic Drug Delivery System, Extra Strength, 8-HOUR Average Wear Time, 6/1-patch pouches/box. Dosage: 120mA/min.
Quantity: 5,141 primary cartons
Why Was This Recalled?
The dosage information on the pouch is incorrect; the primary carton label is correct.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Tapemark Company
Tapemark Company has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report