Noven Pharmaceuticals, Inc. recalls Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches Rx Only NDC
Noven Pharmaceuticals recalls Daytrana (methylphenidate transdermal system) due to adhesive issues that could lead to incorrect drug delivery. This medication is prescription-only and contains 30 patches delivering 10 mg over 9 hours.
Lower-risk recall
Defective Delivery System: Out of specification for adhesive transfer.
Contact the company & request your remedy
What happened, in plain English
Noven Pharmaceuticals is recalling Daytrana patches because the adhesive may not transfer medication properly. This could lead to incorrect drug levels, which might affect treatment effectiveness for ADHD. Read more at govinfonow.com/recall/40625-noven-daytrana-patches-defective-adhesive-may-cause-incorrect-drug-delivery.
Source Summary by GovInfoNow · govinfonow.com/recall/40625-noven-daytrana-patches-defective-adhesive-may-cause-incorrect-drug-delivery · Updated October 7, 2026 · FDA enforcement record: FDA #D-0627-2018
Cite this page
“Noven Daytrana patches: Defective adhesive may cause incorrect drug delivery.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40625-noven-daytrana-patches-defective-adhesive-may-cause-incorrect-drug-delivery. Based on FDA recall #D-0627-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0627-2018%22&limit=1).
Why it’s dangerous
The adhesive in the Daytrana patches may not transfer medication correctly, leading to inconsistent drug delivery. This could cause the medication to not work as intended, potentially affecting ADHD treatment.
Who’s affected
People prescribed Daytrana for ADHD who have the specific lot number (82237) from the recall batch. Those using the medication as directed are most at risk if the adhesive fails.
How to tell if you have this one
Check for the lot number 82237 on the packaging. The product contains 30 patches that deliver 10 mg over 9 hours and is prescription-only.
- Brand
Noven- Category
Drug
What to do — step by step
Check Product Details
Look for the lot number 82237 on the packaging to confirm if your Daytrana patches are affected.
Questions people ask
Is this product safe to use?
The recall is due to potential adhesive issues that could affect drug delivery, but the product is safe to use if the adhesive works correctly. The manufacturer has not issued a stop-use order.
How can I get a replacement?
The recall record does not specify a replacement process or contact for affected customers.
What should I do if I have the recalled product?
The recall record does not state any specific action steps beyond checking the lot number. Contact Noven Pharmaceuticals at 1-877-567-7857 for further assistance.
Contact Noven
We’ve drafted a message you can send Noven to request your refund or repair — edit it as you like.
Subject: Recall D-0627-2018 — Noven Noven Hello, I own a Noven that is covered by recall D-0627-2018 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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Where this comes from
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.
- Official source: FDA Recall #D-0627-2018 (April 9, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0627-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.