Drugs & medicalClass II

Dr. Reddy's Laboratories, Inc. recalls Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, a) 30 count (NDC 43598-743-30), b) 90 count (NDC 43598-743-90)…

Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity

Read the official notice →
Date
2021-11-10
Country
United States
Brand
Dr. Reddy's Laboratories
Product
Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, a) 30 count (NDC 43598-743-30), b) 90 count (NDC 43598-743-90) bottles, Rx…
Classification
Class II
Units
Nationwide in the US
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2022-03-02
  2. US
  3. 2022-01-26
  4. US
  5. US
  6. 2021-12-15
  7. US
  8. 2021-11-10
  9. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, 500 count bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories…

    Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10 mg were found in…

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide in the USOfficial notice →
  10. 2021-10-27
  11. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Omeprazole Delayed-Release Capsules, 20 mg* (equivalent to 20.6 mg omeprazole magnesium), 24 Hour, 14-count capsules per bottle…

    CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.

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

Other drugs & medical recalls in the United States

  1. 2021-11-10
  2. US
    Drugs & medicalClass I

    Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals recalls Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c)…

    Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets

    FDA · DrugBryant Ranch Prepack, Inc. dba BRP PharmaceuticalsNationwide in the USOfficial notice →
  3. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09)…

    CGMP Deviations: impurity N-nitrosoirbesartan detected in API

    FDA · DrugLupin Pharmaceuticals Inc.Product was distributed to major distributors who may have further distributed…Official notice →
  4. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, 500 count bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories…

    Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10 mg were found in…

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide in the USOfficial notice →
  5. 2021-11-03
  6. US
    Drugs & medicalClass II

    Elekta, Inc. recalls Oncentra Brachy users using version 4.0 and above with Applicator Modeling license 170283-00

    Under certain circumstances, there can be a difference between the planned and delivered dose of the two ovoid channels.

    FDA · DeviceElekta, Inc.Distribution throughout USA OUS distribution including:Algeria, Argentina,…Official notice →
  7. US
    Drugs & medicalClass II

    Siemens Healthcare Diagnostics, Inc. recalls Advia Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP), SMN 11319151

    The firm has confirmed the potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein reagent carryover impacting Enzymatic Hemoglobin A1c (A1c_E and A1c_EM) results. Falsely depressed Enzymatic Hemoglobin A1c…

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide distribution - US Nationwide distribution.Official notice →
  8. US
    Drugs & medicalClass II

    Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP), SMN 11097543

    The firm has confirmed the potential for Atellica CH Urinary/Cerebrospinal Fluid Protein reagent carryover impacting Enzymatic Hemoglobin A1c (A1c_E and A1c_EM) results. Falsely depressed Enzymatic Hemoglobin A1c…

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide distribution - US Nationwide distribution.Official notice →
See all drugs & medical recalls →