Drugs & medicalClass II

Noven Pharmaceuticals Inc recalls Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for…

Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.

Read the official notice →
Date
2022-07-06
Country
United States
Brand
Noven Pharmaceuticals
Product
Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for…
Classification
Class II
Units
Distributed Nationwide in the USA
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Noven Pharmaceuticals recalls

  1. 2024-11-27
  2. US
    Drugs & medicalClass II

    Noven Pharmaceuticals Inc recalls Xelstrym (dextroamphetamine) transdermal system, 13.5 mg dextroamphetamine/9 hours, 30 individually sealed transdermal patches, inside…

    Defective Delivery System: The product does not meet predetermined specifications for Coldflow (adhesive).

    FDA · DrugNoven Pharmaceuticals IncUSA nationwide.Official notice →
  3. 2023-03-29
  4. US
    Drugs & medicalClass II

    Noven Pharmaceuticals Inc recalls Daytrana (methylphenidate transdermal system) CII, 30 mg, 30-count carton, Rx only, Manufactured for Noven Therapeutics, LLC., Miami by…

    Defective Delivery System: Out of specification for shear.

    FDA · DrugNoven Pharmaceuticals IncUS NationwideOfficial notice →
  5. 2022-12-07
  6. US
    Drugs & medicalClass II

    Noven Pharmaceuticals Inc recalls Daytrana (methylphenidate transdermal system), Delivers 15 mg over 9 hours, (1.6 mg/hr), 30 patches per box, Rx only, Manufactured for…

    Defective Delivery System: Recalled lot was found to be out of specification for shear. Shear is an attribute related to the adhesive properties of the transdermal patches.

    FDA · DrugNoven Pharmaceuticals IncNationwide in the USAOfficial notice →
  7. 2022-06-01
  8. US
    Drugs & medicalClass II

    Noven Pharmaceuticals Inc recalls Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for…

    Defective Delivery System: customer complaints exceeded respective action limits.

    FDA · DrugNoven Pharmaceuticals IncNationwide to the U.S. MarketOfficial notice →
All 5 Noven Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2022-07-06
  2. US
    Drugs & medicalClass II

    Akorn, Inc. recalls Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass bottle, Rx only, Manufactured by: HI-TECH PHARMACAL…

    Defective container: defect prevents product from dispensing as intended.

    FDA · DrugAkorn, Inc.Nationwide USAOfficial notice →
  3. US
  4. US
    Drugs & medicalClass II

    Akorn, Inc. recalls Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only, 60 mL (2 fl. oz.) bottle, Manufactured by: HI-TECH PHARMACAL CO., INC.,…

    Defective Delivery System: Potential defect that could prevent the product from dispensing as intended.

    FDA · DrugAkorn, Inc.Nationwide in the U.S.Official notice →
  5. US
    Drugs & medicalClass I

    Akcea Therapeutics, Inc. recalls Tegsedi (inotersen) Injection 284 mg/1.5 mL, Rx Only, Sterile solution for Subcutaneous Use, 4 prefilled syringes, each containing 284…

    Superpotent: High Out of specification (OOS) test result for percent label claim (%LC).

    FDA · DrugAkcea Therapeutics, Inc.KY, USAOfficial notice →
  6. US
    Drugs & medicalClass I

    Green Pharmaceuticals, Inc. recalls SnoreStop NasoSpray, 0.3 FL OZ (9 mL), Green Pharmaceuticals Inc. Camarillo, CA 93012, NDC 61152-199-99, UPC 7 69682 29101 3

    Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain microbial contamination identified as Providencia rettgeri.

    FDA · DrugGreen Pharmaceuticals, Inc.Nationwide within the United StatesOfficial notice →
  7. US
    Drugs & medicalClass II

    Macleods Pharma Usa Inc recalls Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # 33342-052-07, NDC #33342-052-10 & NDC #…

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

    FDA · DrugMacleods Pharma Usa IncProduct was distributed nationwide.Official notice →
See all drugs & medical recalls →