Home / Recalls / Medical Devices
Tapemark Company recalls iontoPATCH On-the-Go Patch Therapy, Transdermal Iontophoretic Drug Delivery System, Extra Strength, 8-HOUR Average Wear
Recalled January 12, 2022 · FDA recall Z-0454-2022 · Tapemark
Hazard
The dosage information on the pouch is incorrect; the primary carton label is correct. · FDA Class III
Units
5,141 primary cartons
Sold at
US Nationwide distribution in the states of CA, FL, IL, MO, NY, OH, and TN.
Description
The dosage information on the pouch is incorrect; the primary carton label is correct.
Product
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.
Manufacturer(s)
Tapemark Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →