Recall Atlas
Drugs & medicalClass II

Dr. Reddy's Laboratories, Inc. recalls Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA…

Presence of foreign substance.

Read the official notice →
Date
2024-07-10
Country
United States
Brand
Dr. Reddy's Laboratories
Product
Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106…
Classification
Class II
Units
IL, MS, 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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2024-11-06
  2. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Cinacalcet Tablets, 90 mg, 30-count bottle, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India., NDC…

    CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit

    FDA · DrugDr. Reddy's Laboratories, Inc.USA Nationwide.Official notice →
  3. 2024-09-04
  4. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls IBU Ibuprofen Tablets, USP, 800 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC…

    Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide in the USA and Puerto RicoOfficial notice →
  5. 2024-08-14
  6. US
    Drugs & medicalClass III

    Dr. Reddy's Laboratories, Inc. recalls Sevelamer Carbonate for Oral Suspension 0.8g packets, packaged in 90 packets per container, Distributor: Dr. Reddy's Laboratories…

    Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide within the United StatesOfficial notice →
  7. 2024-07-10
  8. 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 →
  9. 2024-06-05
  10. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Zoledronic Acid Injection 5mg/100mL Sterile Solution, 100mL Single-Dose vials, Rx only, Distributor: Dr. Reddy's Laboratories…

    Lack of Assurance of Sterility: Leaking vials

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide within the United StatesOfficial notice →
  11. 2024-05-29
  12. US
    Drugs & medicalClass III

    Dr. Reddy's Laboratories, Inc. recalls Sirolimus Tablets 1mg Tablets 100-count bottle, Rx Only, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made…

    Failed Impurities/Degradation Specifications

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

Other drugs & medical recalls in the United States

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

    Horiba Instruments Incorporated recalls HORIBA custom configured fluorescence instrument, modular Fluorolog-QM

    HORIBA custom configured fluorescence instrument has a laser safety defect. This custom configuration of the modular Instrument removed the primary light source and the excitation monochromator. A plastic cap was…

    FDA · DeviceHoriba Instruments IncorporatedUS Nationwide and Worldwide DistributionOfficial notice →
  3. US
    Drugs & medicalClass I

    Integrity Products recalls RAM IT, Horny Goat Weed, dietary supplement capsules, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By:…

    Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

    FDA · DrugIntegrity ProductsNationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass II

    The Harvard Drug Group LLC dba Major Pharmaceuticals and… recalls Venlafaxine Hydrochloride, extended-release capsules, USP, 37.5mg, 10 x 10 blister card in one carton,…

    Failed dissolution specifications: out of specification result obtained during routine stability testing for high dissolution.

    FDA · DrugThe Harvard Drug Group LLC dba Major Pharmaceuticals and…Nationwide. No foreign consignees.Official notice →
  5. 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 →
  6. 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 →
  7. 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 →
See all drugs & medical recalls →