Recall Atlas
Drugs & medicalClass II

Trigen Laboratories recalls Methylphenidate Hydrochloride, Extended-release Tablets, USP, 36mg, 100-count Bottle, Rx Only, Manufactured for: Trigen Laboratories, LLC,…

Failed dissolution specifications: this product is being recalled due to this batch not meeting dissolution specifications.

Read the official notice →
Date
2024-07-10
Country
United States
Brand
Trigen Laboratories
Product
Methylphenidate Hydrochloride, Extended-release Tablets, USP, 36mg, 100-count Bottle, Rx Only, Manufactured for: Trigen Laboratories, LLC,…
Classification
Class II
Units
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2024-07-10
  2. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Decitabine for Injection 50mg per vial, For intravenous infusion only Cytotoxic Agent, Sterile, Rx Only, Single-Dose Vial,…

    CGMP Deviations: Out of Specification for Total Aerobic Microbial Count (TAMC) test for unfiltered bulk for decitabine for injection.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide in the USAOfficial notice →
  3. US
    Drugs & medicalClass III

    Dr. Reddy's Laboratories, Inc. recalls Eszopiclone Tablets, USP 1mg CIV, 30-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachupally - 500 090…

    Failed Impurities/Degradation Specifications: Related Substances

    FDA · DrugDr. Reddy's Laboratories, Inc.OH, MSOfficial notice →
  4. US
    Drugs & medicalClass III

    Accord Healthcare, Inc. recalls Dodex Injectable (Cyanocobalamin Injection) USP, 1,000mcg/mL, 1mL multiple dose vial, Rx only, Manufactured for: Accord Healthcare, Inc.,…

    Subpotent drug: out of specification results

    FDA · DrugAccord Healthcare, Inc.USA NationwideOfficial notice →
  5. US
    Drugs & medicalClass II

    Little Moon Essentials LLC recalls Little Moon Essentials, Crampy Belly Rub (Camphor 1.1%), Packaged as a) 4 FL OZ (118ML) glass jar, UPC Code 6 73673 88260 2, NDC…

    CGMP deviations

    FDA · DrugLittle Moon Essentials LLCNationwide USA and Ontario, Canada (2 retailers)Official notice →
  6. US
    Drugs & medicalClass II

    Medisca Inc. recalls Budesonide, USP (Micronized), 500 mg, White to off-white odorless, crystalline powder, Medisca Inc., Plattsburgh, NY, 12901, USA, NDC:…

    CGMP Deviations and Presence of Particulate Matter: Glass

    FDA · DrugMedisca Inc.Nationwide in the USA and CanadaOfficial notice →
  7. 2024-07-03
  8. US
    Drugs & medicalClass II

    Cook Incorporated recalls Ultrathane Mac-Loc Locking Loop Multipurpose Drainage Catheter ULT16.0-38-25-P-6S-MCL-HC--Intended for percutaneous drainage in a variety…

    Product labels state the incorrect expiration dates that extends beyond their true expiration date

    FDA · DeviceCook IncorporatedMA Foreign: Spain, and NetherlandsOfficial notice →
See all drugs & medical recalls →