Drugs & medicalClass II

Dr. Reddy's Laboratories, Inc. recalls Lansoprazole Delayed-Release Orally Disintegrating Tablets, 30 mg, 10 Packs of 10 Tablets each, 100 Tablets per blister pack, Rx…

Failed Dissolution Specifications

Read the official notice →
Date
2022-05-11
Country
United States
Brand
Dr. Reddy's Laboratories
Product
Lansoprazole Delayed-Release Orally Disintegrating Tablets, 30 mg, 10 Packs of 10 Tablets each, 100 Tablets per blister pack, Rx Only,…
Classification
Class II
Units
OH
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Dr. Reddy's Laboratories recalls

  1. 2022-12-07
  2. US
  3. 2022-10-12
  4. US
    Drugs & medicalClass III

    Dr. Reddy's Laboratories, Inc. recalls Phytonadione Injectable Emulsion USP, 10 mg/mL, 25x 1 mL single dose ampules per carton, Rx only, Distributed by: Dr. Reddy's…

    Failed Stability Specifications: Out of specification results reported at 12-month stability testing for aluminum content.

    FDA · DrugDr. Reddy's Laboratories, Inc.USA nationwideOfficial notice →
  5. 2022-08-03
  6. US
  7. 2022-04-06
  8. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Lansoprazole Delayed-Release Capsules, USP, 30 mg, 90-count bottle, Rx Only, Manufactured By: Dr. Reddy's Laboratories Limited,…

    Failed Dissolution Specifications; during long term stability testing.

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide in the USAOfficial notice →
  9. US
    Drugs & medicalClass III

    Dr. Reddy's Laboratories, Inc. recalls Atorvstatin Calcium Tablets, USP 80 mg*, 90 Tablets, Rx Only, Mrd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409,…

    Failed Impurities/Degradation Specifications: Out of Specification results for related substance.

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide in the USA.Official notice →
  10. 2022-03-02
  11. US
    Drugs & medicalClass III

    Dr. Reddy's Laboratories, Inc. recalls Sapropterin Dihydrochloride Powder for Oral Solution, 100 mg, 30 individual packets per carton, Rx Only, Dr. Reddy's,…

    Subpotent Drug: Out-of-specification results observed in Assay in sapropterin dihydrochloride powder 100mg.

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide in the USA.Official notice →
All 35 Dr. Reddy's Laboratories recalls →

Other drugs & medical recalls in the United States

  1. 2022-05-11
  2. US
    Drugs & medicalClass II

    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion systems with software release R1.x

    In the Azurion system, the user can add a new study to a patient by selecting the option Add Study . The Add Study dialogue box is then displayed where the Patient Type is selected to perform the study. Due to a…

    FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.US Nationwide and Worldwide DistributionOfficial notice →
  3. US
    Drugs & medicalClass I

    Best Brands Consumer Products, Inc. recalls The Mandalorian Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./60 mL bottles, Best Brands Consumer Products, Inc., c/o Best…

    Chemical Contamination; FDA analysis found product to contain benzene

    FDA · DrugBest Brands Consumer Products, Inc.Nationwide in the USOfficial notice →
  4. US
    Drugs & medicalClass I

    Best Brands Consumer Products, Inc. recalls Mickey Mouse Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./to mL bottle, Best Brands Consumer Products, Inc., c/o Best Brands…

    Chemical Contamination; FDA analysis found product to contain methanol

    FDA · DrugBest Brands Consumer Products, Inc.Nationwide in the USOfficial notice →
  5. US
  6. US
    Drugs & medicalClass II

    McKesson Corporation dba McKesson Drug Company recalls Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL bottle, Rx only, Manufactured by: Teligent…

    CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.

    FDA · DrugMcKesson Corporation dba McKesson Drug CompanyNationwide in the United States including Guam and the Northern Mariana Islands.Official notice →
  7. US
    Drugs & medicalClass III

    Akorn, Inc. recalls Lidocaine Hydrochloride Oral Topical Solution, USP (Viscous) 2%, 100 mL per bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co., Inc.…

    Failed viscosity specification - product was below specificcation

    FDA · DrugAkorn, Inc.Nationwide USA and Puerto RicoOfficial notice →
See all drugs & medical recalls →