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.

Read the official notice →
Date
2022-06-01
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
Nationwide to the U.S. Market
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2022-07-06
  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 received for ripping patches and tight release/adhesive transfer.

    FDA · DrugNoven Pharmaceuticals IncDistributed Nationwide in the USAOfficial notice →
All 5 Noven Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2022-06-01
  2. US
    Drugs & medicalClass II

    Direct Rx recalls Losartan Pot/HCTZ 100/12.5 mg 90 Tabs NDC 72189-290-90 Packaged and Distributed By: Direct Rx Dawsonville, GA 30534 Mfg. For Macleods…

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

    FDA · DrugDirect RxFLOfficial notice →
  3. US
    Drugs & medicalClass II

    Preferred Pharmaceuticals, Inc. recalls Losartan Potassium & HCTZ Tablets 50mg/12.5 mg, hydrochlorothiazide USP 12.5, Pkg Size: 90, NDC: 68788-7758-09.

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

    FDA · DrugPreferred Pharmaceuticals, Inc.Within the U.S in FL and CA.Official notice →
  4. US
    Drugs & medicalClass III

    Eco Lips, Inc recalls Higher Education Make Out Ready Vegan Lip Balm, SPF 15, Net Wt. 0.15 oz (4.25 g) per tube, Active Ingredients: Oxtinoxate (7.5%),…

    Mislabeling: The active ingredient list on the label does not match the product's actual ingredients Specifically, the label states Octinoxate 7.5% and Oxybenzone 3%, while the product therein is made with Octinoxate…

    FDA · DrugEco Lips, IncCAOfficial notice →
  5. US
    Drugs & medicalClass II

    Direct Rx recalls Zonisamide Capsules USP, 100 mg, 90-count bottle, Rx Only, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, Manufactured for:…

    CGMP Deviations: Gaps in the quality system in the Quality Control microbiology laboratory.

    FDA · DrugDirect RxNationwide to the U.S. marketOfficial notice →
  6. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Losartan HCTZ 100/25 mg, 90 count bottles NDC# 70518-2578-00 Repackaged NDC Original NDC # 68180-0217-09

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

    FDA · DrugRemedyRepack Inc.Product was distributed to FL, SC and VAOfficial notice →
  7. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Losartan HCTZ 50/12.5 mg, 90 count bottle Original NDC# 33342-0050-10 Repackaged NDC# 70518-3231-00

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

    FDA · DrugRemedyRepack Inc.Recalled product was distributed to Florida.Official notice →
See all drugs & medical recalls →