Tapemark recalls extra strength iontoPATCH patches due to incorrect dosage information on pouches. The primary carton label is correct. Consumers should check lot numbers 1131-1 and :1131-2.
The dosage information on the pouch is incorrect; the primary carton label is correct.
Tapemark is recalling extra strength iontoPATCH patches because the dosage information on the pouches is incorrect. The primary carton label is correct, but the pouches may lead to improper medication use if not followed carefully.
The pouches have incorrect dosage information (120mA/min.) that could lead to improper medication use. The primary carton label is correct, but the pouches may be misread by users.
Owners of Tapemark iontoPATCH Extra Strength patches with lot numbers 1131-1 or 1131-2 are affected. People using these patches for medication delivery are most at risk of incorrect dosing.
Check for lot numbers 1131-1 or 1131-2 on the pouches. The product is an extra strength iontoPATCH patch with 8-hour average wear time.
Look for lot numbers 1131-1 or 1131-2 on the pouches.
The dosage information on the pouches is incorrect; the primary carton label is correct.
Lot numbers 1131-1 and 1131-2.
Yes, the primary carton label is correct.
We’ve drafted a message you can send Tapemark to request your refund or repair — edit it as you like.
Subject: Recall Z-0454-2022 — Tapemark Tapemark Hello, I own a Tapemark that is covered by recall Z-0454-2022 from Tapemark. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
