Noven Pharmaceuticals recalls Daytrana (methylphenidate transdermal system) 30mg 30-count cartons with defective delivery system. Affected lots expire 3/2023 to 10/2023. Stop using immediately if you have these products.
Defective Delivery System: Out of specification for shear.
Noven Pharmaceuticals is recalling Daytrana (methylphenidate transdermal system) 30mg 30-count cartons due to a defective delivery system that may not function properly. This could lead to inconsistent medication delivery, potentially causing treatment failure or adverse effects.
The delivery system is out of specification for shear, meaning it may not release medication properly. This could cause inconsistent dosing, leading to treatment failure or unexpected medication effects.
People with prescriptions for Daytrana 30mg 30-count cartons from Noven Pharmaceuticals. Those who have the specific lots listed in the recall (expiring 3/2023 to 10/2023) are most at risk.
Check your Daytrana 30mg 30-count carton for the lot numbers listed: 91474, 91959 (expiring 3/2023), 91958 (expiring 6/2023), 92478 (expiring 7/2023), 92479 & 92198 (expiring 8/2023), 92199 and 93040 (expiring 9/2023), 93041 (expiring 10/2023).
Look for the lot numbers listed in the recall: 91474, 91959, 91958, 92478, 92479, 92198, 92199, 93040, 93041.
If you have the recalled lot numbers, stop using the Daytrana product immediately.
The delivery system is out of specification for shear, which may cause inconsistent medication release.
Check your Daytrana 30mg 30-count carton for the lot numbers listed: 91474, 91959, 91958, 92478, 92479, 92198, 92199, 93040, 93041.
The recall record does not specify a return process or remedy.
We’ve drafted a message you can send Noven to request your refund or repair — edit it as you like.
Subject: Recall D-0473-2023 — Noven Noven Hello, I own a Noven that is covered by recall D-0473-2023 from Noven. 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.
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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.
