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.

Read the official notice →
Date
2022-04-06
Country
United States
Brand
Dr. Reddy's Laboratories
Product
Atorvstatin Calcium Tablets, USP 80 mg*, 90 Tablets, Rx Only, Mrd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409, INDIA, NDC…
Classification
Class III
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

More Dr. Reddy's Laboratories recalls

  1. 2022-08-03
  2. US
  3. 2022-05-11
  4. US
  5. 2022-04-06
  6. 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 →
  7. 2022-03-02
  8. 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 →
  9. US
  10. 2022-01-26
  11. US
All 35 Dr. Reddy's Laboratories recalls →

Other drugs & medical recalls in the United States

  1. 2022-04-06
  2. US
    Drugs & medicalClass II

    Aurolife Pharma, LLC recalls Glycopyrrolate Tablets, USP, 1 mg, 100-count bottle, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road,…

    Presence of Foreign Substance: Complaint for pieces of glass discovered in a sealed bottle which came from equipment within the packaging room.

    FDA · DrugAurolife Pharma, LLCNationwide in the USA and Puerto RicoOfficial notice →
  3. US
    Drugs & medicalClass II

    Drug Depot, Inc., dba APS Pharmacy recalls TESTOSTERONE CYPIONATE/ ANASTROZOLE *GS* OIL (10ML) 200MG/0.5MG/ML; Packaged in a multi dose 10ML vial, as a) (CA) 4 ML…

    Lack of sterility assurance.

    FDA · DrugDrug Depot, Inc., dba APS PharmacyNationwide in the USA including Puerto Rico.Official notice →
  4. US
    Drugs & medicalClass III

    Taro Pharmaceuticals U.S.A., Inc. recalls Clotrimazole and Betamethasone Dipropionate Cream USP, 1%/0.05%,15 g tubes, Rx only, Manufactured by: Taro Pharmaceuticals…

    Failed Content Uniformity Specifications: Out-of-specification result for the Betamethasone Dipropionate assay of a stability sample

    FDA · DrugTaro Pharmaceuticals U.S.A., Inc.Product was distributed to one retail consignee in NY.Official notice →
  5. 2022-03-31
  6. US
    Drugs & medical

    Maped Helix USA Recalls Metal Lockable Drug Chests Due to Risk of Poisoning

    The locking mechanism can fail allowing access to the contents inside the chest, posing a risk of poisoning.

    CPSCAbout 7,700Official notice →
  7. 2022-03-30
  8. US
    Drugs & medicalClass II

    Dignitana, Inc. recalls DigniCap Delta Scalp Cooling System, Product Number: 900-1001, Labeling: The DigniCap Scalp Cooling System User Manual (PN:…

    Instructions for Use (IFUs) updated to include use of a headband is now recommended for all patients and instructions for the application of the headband. Additionally, IFU updated to include warnings for risk of…

    FDA · DeviceDignitana, Inc.US Distribution to states of: LA, NC, NJ, FL, WI, CA, NY, KS, GA, SC, CT and KY.Official notice →
  9. US
    Drugs & medicalClass III

    Cytocell Ltd. recalls Cytocell 8 Square Template Slides (Glass)- microscope slides Reference: PCN008

    Labelled with an incorrect expiry date on the outer label with an extended expiry date than the validated shelf life. The correct expiry date for the device is 2022-02 and not 2023-05 as shown on the outer label.

    FDA · DeviceCytocell Ltd.US Nationwide distribution in the states of CT, TX.Official notice →
See all drugs & medical recalls →