Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Low RiskFDA Drug
Medications & Supplements/Over-the-Counter

Walgreens Mucus Relief D Tablets Recalled for Subpotency

Agency Publication Date: January 19, 2022
Share:
Sign in to monitor this recall

Summary

Dr. Reddy's Laboratories, Inc. has recalled approximately 18,336 cartons of Walgreens brand Mucus Relief D (Guaifenesin and Pseudoephedrine HCl ER) Tablets, 600 mg/60mg. The recall was initiated because the medication was found to be subpotent, meaning it contains less than the required amount of active ingredients. There have been no reports of incidents or injuries related to this recall. Consumers should contact their healthcare provider or pharmacist if they have concerns about the effectiveness of this medication.

Risk

Subpotency means the medication may not contain the full strength of ingredients needed to treat symptoms. This could lead to a failure to relieve chest congestion and sinus pressure as effectively as expected.

What You Should Do

  1. The recalled products are 36-count cartons of Walgreens Mucus Relief D (Guaifenesin and Pseudoephedrine HCl ER) 600 mg/60mg Tablets, identified by NDC 0363-164-3.
  2. Check the carton for lot numbers AT2102065A or AT2102065B with an expiration date of April 2023 (04/2023).
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Dr. Reddy's Laboratories, Inc. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Mucus Relief D (Guaifenesin Pseudoephedrine HCl ER Tablets) (36-count)by Walgreens
Variants: 600 mg/60mg, ER Tablets, Blister pack
Lot Numbers:
AT2102065A (Exp 04/2023)
AT2102065B (Exp 04/2023)
NDC:
0363-164-3

Distributed by Walgreen Co.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 89388
Status: Resolved
Manufacturer: Dr. Reddy's Laboratories, Inc.
Sold By: Walgreens; Walgreen Co.
Manufactured In: India
Units Affected: 18336 cartons
Distributed To: Nationwide

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.