Drugs & medicalClass III

Dr. Reddy's Laboratories, Inc. recalls Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons,…

Subpotent drug

Read the official notice →
Date
2022-01-26
Country
United States
Brand
Dr. Reddy's Laboratories
Product
Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons,…
Classification
Class III
Units
USA Nationwide
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2022-04-06
  2. 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 →
  3. 2022-03-02
  4. 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 →
  5. US
  6. 2022-01-26
  7. US
  8. 2021-12-15
  9. US
  10. 2021-11-10
  11. 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 →
All 35 Dr. Reddy's Laboratories recalls →

Other drugs & medical recalls in the United States

  1. 2022-01-26
  2. US
    Drugs & medicalClass I

    ev3 Inc. recalls Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-M and H1-M-INT., Multi-vessel, 6F (2.2 mm) Recommended sheath, 0.014"…

    Reports have been received of tip damage during use of the devices which resulted in some instances of tip detachment and embolization.

    FDA · Deviceev3 Inc.Worldwide Distribution: US (nationwide), including PR; and Foreign…Official notice →
  3. US
    Drugs & medicalClass I

    Mylan Pharmaceuticals Inc recalls Semglee (insulin glargine) injection, 100 units/mL (U-100), 3 mL Prefilled Pen (NDC 49502-0196-71), packaged in Five 3 mL Prefilled…

    Labeling: Missing Label: label missing from some Semglee prefilled pens.

    FDA · DrugMylan Pharmaceuticals IncNationwide in the USA and Thailand.Official notice →
  4. US
    Drugs & medicalClass II

    Medique Products recalls Physicians CARE Extra Strength PAIN RELIEVER [Acetaminophen, Aspirin (NSAID), and Caffeine], 250 mg, 250 mg, 65 mg, packaged as 100-count…

    CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.

    FDA · DrugMedique ProductsNationwide in the USAOfficial notice →
  5. US
    Drugs & medicalClass II

    Mayne Pharma Inc recalls Lexette (halobetasol propionate) Topical Foam, 0.05% 50 g canisters, Rx ONLY, Distributed by: Mayne Pharma Greenville, NC 27834, NDC…

    CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid instead of foam.

    FDA · DrugMayne Pharma IncNationwide within the United StatesOfficial notice →
  6. US
  7. US
    Drugs & medicalClass I

    Lohxa, LLC recalls SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton, Mfg for: AvKARE, TN 38478, NDC 50262-731-24.

    Microbial Contamination of Non-Sterile Product

    FDA · DrugLohxa, LLCProduct was distributed to one wholesale who further distributed the product…Official notice →
See all drugs & medical recalls →