Tapemark Company iontoPATCH On-the-Go Patch Therapy, Transdermal Iontophoretic Drug Delivery recall — FDA Z-0454-2022
The dosage information on the pouch is incorrect; the primary carton label is correct.
Overview of recall records associated with Tapemark Company, including dates, categories and classifications where available.
Classification mix: Class III: 1.
The dosage information on the pouch is incorrect; the primary carton label is correct.
This page summarizes recall records in which the official source identifies Tapemark Company as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.