The Recall Desk
ModerateFDA (Drugs)·D-0274-2022·Announced 2021-12-15

Walmart Allergy Relief D Extended-Release Tablets Recalled for Failed Dissolution

Dr. Reddy's Laboratories is recalling Walmart brand Allergy Relief D extended-release tablets (Lot #AC2103329B) nationwide because the tablets failed to meet dissolution specifications, which may affect medication effectiveness.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: This is an FDA Class III recall for a manufacturing/quality defect (failed dissolution specifications) with no reported illnesses or injuries. The hazard is theoretical—potential reduced efficacy—making this a precautionary recall appropriate for a Moderate severity rating.

Plain-English summary

Dr. Reddy's Laboratories, Inc. is recalling Allergy Relief D Fexofenadine HCl 60 mg / Pseudoephedrine HCl 120 mg Extended-Release Tablets, USP, distributed by Walmart Inc. The recall affects 9,984 cartons of 30-tablet bottles (NDC 49035-273-30) distributed nationwide in the USA.

The recall was initiated because the tablets failed to meet dissolution specifications. Dissolution specifications ensure that medication dissolves properly in the body at the intended rate, allowing the active ingredients to be absorbed as designed.

Consumers who have purchased this product should stop using it and consult their healthcare provider or pharmacist about obtaining a replacement or alternative medication. The affected lot number is AC2103329B, and the product was manufactured in India.

The recalled product

Product
Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, USP, 30 Extended-Release Tablets USP, Distributed By Walmart Inc., Bentonville, AR 72716, Product of India, NDC 49035-273-30.
Manufacturer
Dr. Reddy's Laboratories, Inc.
Category
Drug — Allergy / Decongestant
Hazard
Affected units
9,984

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot #: AC2103329B

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 9 recalled by Dr. Reddy's Laboratories, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 9 products in this recall →

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Same manufacturer · Dr. Reddy's Laboratories, Inc.

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Same hazard · dissolution failure

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